| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:10212820-10213434 | Common:5; Rare:136 | ||||
| chr12:10307774-10307908 | Common:1; Rare:17 | ||||
| chr12:10613473-10613686 | Common:1; Rare:84 | ||||
| chr12:10722840-10723022 | Common:3; Rare:59 | ||||
| chr12:10929125-10929273 | Common:1; Rare:40 | ||||
| chr12:11171076-11171286 | Common:3; Rare:71 | ||||
| chr12:11171541-11171760 | Common:4; Rare:74 | ||||
| chr12:11269700-11269957 | Common:1; Rare:45 | ||||
| chr12:11649774-11650111 | Common:1; Rare:98 | ||||
| chr12:12267205-12267383 | Common:5; Rare:78 | ||||
| chr12:12356981-12357187 | Common:4; Rare:108 | ||||
| chr12:12561143-12561263 | Common:1; Rare:23 | ||||
| chr12:12562205-12562369 | Rare:48 | ||||
| chr12:12611789-12612153 | Common:2; Rare:102 | ||||
| chr12:12717189-12717502 | Rare:108; Clinvar:2; Clinvar (benign):1 |