| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:26833187-26833440 | Common:1; Rare:75 | ||||
| chr12:26937932-26938103 | Common:6; Rare:55 | ||||
| chr12:26938319-26938534 | Common:3; Rare:83 | ||||
| chr12:27244010-27244328 | Common:2; Rare:104 | ||||
| chr12:27523990-27524244 | Rare:61 | ||||
| chr12:27710743-27710879 | Common:2; Rare:63 | ||||
| chr12:28190378-28190483 | Common:1; Rare:30 | ||||
| chr12:30695853-30696084 | Common:2; Rare:53 | ||||
| chr12:31324098-31324251 | Rare:38 | ||||
| chr12:31729015-31729267 | Rare:74 | ||||
| chr12:31959282-31959488 | Common:2; Rare:65 | ||||
| chr12:32679255-32679350 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:32896738-32896999 | Common:4; Rare:85; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:42326031-42326182 | Common:1; Rare:51 | ||||
| chr12:43758753-43758996 | Common:2; Rare:68; Clinvar:2 |