| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:72286924-72287128 | Common:1; Rare:41 | ||||
| chr12:72479305-72479548 | Rare:53 | ||||
| chr12:72575265-72575538 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr12:72634126-72634407 | Common:1; Rare:49 | ||||
| chr12:74538974-74539331 | Common:2; Rare:80 | ||||
| chr12:74539448-74539625 | Common:2; Rare:41 | ||||
| chr12:74539867-74540049 | Rare:44 | ||||
| chr12:74540505-74540544 | Rare:5 | ||||
| chr12:74540625-74541206 | Common:6; Rare:120 | ||||
| chr12:74541224-74541303 | Rare:23 | ||||
| chr12:75484155-75484243 | Rare:14 | ||||
| chr12:76030498-76030762 | Common:1; Rare:114 | ||||
| chr12:76050488-76050569 | Rare:20 | ||||
| chr12:76059796-76060278 | Common:5; Rare:97 | ||||
| chr12:76064810-76064925 | Rare:19 |