| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109573470-109573806 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:110468702-110468909 | Rare:54 | ||||
| chr12:111685867-111686103 | Rare:88 | ||||
| chr12:112013140-112013460 | Common:1; Rare:111 | ||||
| chr12:113185440-113185769 | Common:8; Rare:117 | ||||
| chr12:118136003-118136181 | Common:2; Rare:45 | ||||
| chr12:120201081-120201349 | Common:2; Rare:85 | ||||
| chr12:120446359-120446479 | Common:1; Rare:53 | ||||
| chr12:120469554-120469867 | Common:2; Rare:112 | ||||
| chr12:120495875-120496157 | Common:5; Rare:93 | ||||
| chr12:122526889-122527282 | Common:3; Rare:136 | ||||
| chr12:123233102-123233486 | Common:2; Rare:122; Clinvar:1 | ||||
| chr12:123364828-123364968 | Common:2; Rare:55 | ||||
| chr12:123584336-123584595 | Common:5; Rare:80 | ||||
| chr12:123601819-123602139 | Common:6; Rare:80 |