| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6493212-6493502 | Common:7; Rare:86 | ||||
| chr12:6493718-6494146 | Common:2; Rare:122 | ||||
| chr12:6529581-6529804 | Common:2; Rare:61 | ||||
| chr12:6534355-6534860 | Common:8; Rare:207 | ||||
| chr12:6536483-6536788 | Rare:101 | ||||
| chr12:6563614-6563907 | Common:3; Rare:86 | ||||
| chr12:6568234-6568411 | Rare:70 | ||||
| chr12:6663085-6663442 | Common:2; Rare:101 | ||||
| chr12:6688843-6689089 | Rare:76 | ||||
| chr12:6689441-6689748 | Common:2; Rare:77 | ||||
| chr12:6723834-6724296 | Common:1; Rare:102 | ||||
| chr12:6752967-6753168 | Common:5; Rare:62 | ||||
| chr12:6851902-6852197 | Rare:78 | ||||
| chr12:6867384-6867604 | Common:2; Rare:114; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873281-6873534 | Common:2; Rare:73 |