| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:74537682-74537945 | Common:1; Rare:87 | ||||
| chr12:75334525-75334721 | Rare:49 | ||||
| chr12:75390859-75391463 | Common:2; Rare:212 | ||||
| chr12:75480169-75480235 | Rare:8 | ||||
| chr12:75480731-75480901 | Rare:39 | ||||
| chr12:75481216-75481281 | Rare:13 | ||||
| chr12:75511128-75511207 | Rare:19 | ||||
| chr12:75511524-75511913 | Rare:111 | ||||
| chr12:76031434-76031942 | Common:1; Rare:161 | ||||
| chr12:76083871-76084099 | Rare:62 | ||||
| chr12:76084544-76085129 | Common:7; Rare:167 | ||||
| chr12:76348071-76348159 | Rare:26 | ||||
| chr12:76348282-76348641 | Common:2; Rare:121; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:76558879-76559201 | Common:2; Rare:62 | ||||
| chr12:76559475-76560046 | Common:4; Rare:176 |