| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:96280778-96281017 | Common:1; Rare:59 | ||||
| chr12:98503835-98504016 | Common:2; Rare:51 | ||||
| chr12:98598337-98598714 | Common:2; Rare:82; Clinvar (benign):3 | ||||
| chr12:101317280-101317514 | Rare:54 | ||||
| chr12:101616037-101616171 | Common:2; Rare:23 | ||||
| chr12:101747226-101747255 | Rare:9; Clinvar:3 | ||||
| chr12:101748102-101748410 | Common:1; Rare:41 | ||||
| chr12:101748438-101748611 | Rare:29 | ||||
| chr12:101771145-101771395 | Common:1; Rare:61 | ||||
| chr12:101773360-101773546 | Rare:40 | ||||
| chr12:101796697-101797028 | Common:2; Rare:65; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:103946588-103946941 | Common:1; Rare:91 | ||||
| chr12:105181402-105181455 | Rare:10 | ||||
| chr12:105182083-105182317 | Rare:46 | ||||
| chr12:105183963-105184285 | Common:2; Rare:70 |