| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118016526-118016842 | Common:7; Rare:173 | ||||
| chr12:118061037-118061475 | Common:9; Rare:219 | ||||
| chr12:118061530-118062053 | Common:10; Rare:107 | ||||
| chr12:118062120-118062610 | Common:9; Rare:217 | ||||
| chr12:118062589-118063030 | Common:10; Rare:153 | ||||
| chr12:118103101-118103357 | Common:5; Rare:85 | ||||
| chr12:118103663-118104246 | Common:5; Rare:291 | ||||
| chr12:118135873-118136240 | Common:6; Rare:280 | ||||
| chr12:118372645-118373250 | Common:8; Rare:395 | ||||
| chr12:118376098-118376866 | Common:3; Rare:576 | ||||
| chr12:118376804-118377008 | Common:1; Rare:82 | ||||
| chr12:119178400-119179055 | Common:8; Rare:248; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:119179695-119179865 | Common:1; Rare:39 | ||||
| chr12:119334460-119334840 | Common:2; Rare:83 | ||||
| chr12:119667841-119668095 | Common:4; Rare:110 |