| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:5985012-5985084 | Rare:20; Clinvar:2 | ||||
| chr12:5985562-5985928 | Common:4; Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:5993851-5994627 | Common:5; Rare:209; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:5996522-5996744 | Rare:36 | ||||
| chr12:6006392-6006538 | Rare:25 | ||||
| chr12:6016584-6016832 | Common:1; Rare:92; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:6042915-6043220 | Common:2; Rare:53 | ||||
| chr12:6044076-6044127 | Common:11; Rare:6 | ||||
| chr12:6044194-6044728 | Common:8; Rare:141; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr12:6046700-6047069 | Common:3; Rare:84; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6047341-6047486 | Common:2; Rare:30 | ||||
| chr12:6047701-6047998 | Common:2; Rare:61 | ||||
| chr12:6050127-6050470 | Common:1; Rare:51 | ||||
| chr12:6051473-6051709 | Common:5; Rare:51 | ||||
| chr12:6051756-6051792 | Rare:15 |