| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:10721791-10722122 | Common:1; Rare:86 | ||||
| chr12:10722721-10723065 | Common:3; Rare:104 | ||||
| chr12:10723324-10723473 | Common:4; Rare:44 | ||||
| chr12:11171076-11171250 | Common:1; Rare:61 | ||||
| chr12:11171545-11171693 | Common:2; Rare:46 | ||||
| chr12:12266957-12267166 | Common:3; Rare:85 | ||||
| chr12:12357013-12357300 | Common:6; Rare:127 | ||||
| chr12:12357345-12357396 | Rare:12 | ||||
| chr12:12561096-12561254 | Common:1; Rare:28 | ||||
| chr12:12611814-12612128 | Common:2; Rare:90 | ||||
| chr12:12717104-12717492 | Rare:129; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12725642-12725940 | Common:3; Rare:68 | ||||
| chr12:12891264-12891662 | Common:1; Rare:76 | ||||
| chr12:12979730-12980098 | Common:1; Rare:54 | ||||
| chr12:12989276-12989594 | Rare:86 |