Genomic location | rs number (genotypea) | MAFb | Statistical modelc | Type of variant (gene)d | DNA binding evidencee |
---|---|---|---|---|---|
22:17793969 | rs5749032 (GG) | 40% | Mixture cure | Intergenic | ND |
20:16189263 | rs2327990 (TT) | 11% | Cox proportional hazards | Intergenic | Less likely to affect binding |
3:134513356 | rs11918092 (CC) | 8% | Cox proportional hazards | Intronic (EPHB1) | Minimal binding evidence |
3:134515336 | rs3732568 (AA) | 8% | Cox proportional hazards | Intronic (EPHB1) | Minimal binding evidence |
3:59930672 | rs2366964 (CC) | 8% | Cox proportional hazards | Intronic (FHIT) | ND |
2:6769988 | rs1563948 (AA) | 11% | Cox proportional hazards | Intronic (MIR7515) | Minimal binding evidence |
2:6773920 | rs11694697 (TT) | 11% | Cox proportional hazards | Intronic (MIR7515) | ND |
2:6777992 | rs11692570 (TT) | 11% | Cox proportional hazards | Intronic (MIR7515) | Minimal binding evidence |
2:6779277 | rs2219613 (TT) | 11% | Cox proportional hazards | Intronic (MIR7515) | Minimal binding evidence |
6:91187510 | rs1145724 (GG) | 9% | Cox proportional hazards | Intergenic | Minimal binding evidence |