| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12611581-12612460 | Common:11; Rare:451 | ||||
| chr12:12696068-12696450 | Common:3; Rare:187 | ||||
| chr12:12696470-12696920 | Common:1; Rare:182 | ||||
| chr12:12716925-12717782 | Common:9; Rare:674; Clinvar:8; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr12:12717879-12718821 | Common:4; Rare:522; Clinvar:75; Clinvar (benign):63; Clinvar (pathogenic):4 | ||||
| chr12:12725140-12725546 | Common:6; Rare:202 | ||||
| chr12:12725622-12726121 | Common:10; Rare:218 | ||||
| chr12:12813020-12813425 | Common:4; Rare:212 | ||||
| chr12:12819760-12820450 | Common:4; Rare:100 | ||||
| chr12:12890620-12891100 | Common:3; Rare:197 | ||||
| chr12:12891236-12891979 | Common:7; Rare:246 | ||||
| chr12:12891967-12892765 | Common:16; Rare:418 | ||||
| chr12:13000086-13000590 | Common:7; Rare:332 | ||||
| chr12:13043705-13043815 | Rare:25 | ||||
| chr12:13044237-13044500 | Rare:115 |