| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120446263-120446473 | Common:1; Rare:80 | ||||
| chr12:120469709-120469873 | Common:1; Rare:51 | ||||
| chr12:120495867-120496160 | Common:6; Rare:98 | ||||
| chr12:120687008-120687215 | Common:2; Rare:70 | ||||
| chr12:121888639-121888875 | Common:2; Rare:78 | ||||
| chr12:122526904-122527281 | Common:3; Rare:123 | ||||
| chr12:122872020-122872228 | Rare:33 | ||||
| chr12:122974555-122974809 | Common:1; Rare:56 | ||||
| chr12:122975153-122975314 | Common:1; Rare:67 | ||||
| chr12:122980593-122980966 | Common:2; Rare:106 | ||||
| chr12:123233082-123233490 | Common:3; Rare:137; Clinvar:1 | ||||
| chr12:123436441-123436781 | Common:1; Rare:76 | ||||
| chr12:123584317-123584602 | Common:6; Rare:92 | ||||
| chr12:123584719-123584810 | Common:1; Rare:27 | ||||
| chr12:123633593-123633848 | Common:1; Rare:120; Clinvar:8; Clinvar (benign):1 |