| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12718860-12719574 | Common:1; Rare:437; Clinvar:9; Clinvar (benign):6 | ||||
| chr12:12719512-12720016 | Common:2; Rare:135 | ||||
| chr12:12723803-12725016 | Common:13; Rare:784 | ||||
| chr12:12724925-12725402 | Common:3; Rare:137 | ||||
| chr12:12786297-12787222 | Common:7; Rare:447 | ||||
| chr12:12803252-12803652 | Common:3; Rare:120 | ||||
| chr12:12804535-12804795 | Common:4; Rare:39 | ||||
| chr12:12872180-12872407 | Common:1; Rare:61 | ||||
| chr12:12872430-12872850 | Common:4; Rare:181 | ||||
| chr12:12877780-12878310 | Common:4; Rare:100 | ||||
| chr12:12881458-12881938 | Common:11; Rare:166 | ||||
| chr12:12883182-12883860 | Common:20; Rare:295 | ||||
| chr12:12893087-12893741 | Common:9; Rare:144 | ||||
| chr12:12927403-12927854 | Common:16; Rare:291 | ||||
| chr12:12990773-12991105 | Common:2; Rare:50 |