| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:82358381-82358491 | Rare:46 | ||||
| chr12:88142032-88142368 | Rare:92; Clinvar:3 | ||||
| chr12:89708824-89709097 | Common:1; Rare:106 | ||||
| chr12:101407731-101408051 | Common:2; Rare:79 | ||||
| chr12:102120071-102120201 | Rare:49 | ||||
| chr12:103965698-103965853 | Common:1; Rare:42 | ||||
| chr12:109573488-109573813 | Common:3; Rare:91; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:112013164-112013457 | Common:1; Rare:99 | ||||
| chr12:113185464-113185727 | Common:5; Rare:99 | ||||
| chr12:120201085-120201308 | Common:2; Rare:73 | ||||
| chr12:120495875-120496144 | Common:4; Rare:83 | ||||
| chr12:122526916-122527281 | Common:3; Rare:114 | ||||
| chr12:123233134-123233456 | Common:2; Rare:99; Clinvar:1 | ||||
| chr12:123584317-123584609 | Common:6; Rare:97 | ||||
| chr12:123633640-123633845 | Common:1; Rare:90; Clinvar:8; Clinvar (benign):1 |