| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:75480611-75480804 | Rare:33 | ||||
| chr12:75511556-75511784 | Rare:79 | ||||
| chr12:76083927-76084068 | Rare:44 | ||||
| chr12:76084568-76084878 | Common:1; Rare:103 | ||||
| chr12:76348360-76348480 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76763866-76764261 | Common:5; Rare:163 | ||||
| chr12:76878946-76879221 | Rare:95 | ||||
| chr12:79934924-79935281 | Common:1; Rare:142 | ||||
| chr12:79935335-79935354 | Rare:5 | ||||
| chr12:80937679-80937863 | Common:1; Rare:59 | ||||
| chr12:82358273-82358549 | Common:1; Rare:131 | ||||
| chr12:82358724-82358887 | Common:3; Rare:85 | ||||
| chr12:84912716-84912903 | Common:1; Rare:44 | ||||
| chr12:85280146-85280264 | Common:1; Rare:46 | ||||
| chr12:85280342-85280468 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):1 |