| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:75481220-75481424 | Common:5; Rare:38 | ||||
| chr12:75481441-75481701 | Rare:37 | ||||
| chr12:75511114-75511194 | Rare:19 | ||||
| chr12:75511524-75511917 | Rare:111 | ||||
| chr12:76031406-76031980 | Common:1; Rare:172 | ||||
| chr12:76031991-76032236 | Common:1; Rare:60 | ||||
| chr12:76083894-76084237 | Common:1; Rare:95 | ||||
| chr12:76084455-76085123 | Common:7; Rare:186 | ||||
| chr12:76348064-76348212 | Rare:43; Clinvar (pathogenic):1 | ||||
| chr12:76348303-76348620 | Common:2; Rare:109; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:76558864-76559116 | Common:1; Rare:48 | ||||
| chr12:76559300-76559444 | Rare:18 | ||||
| chr12:76559475-76559644 | Common:2; Rare:45 | ||||
| chr12:76559648-76560025 | Rare:126 | ||||
| chr12:76763827-76764165 | Common:5; Rare:119 |