| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110561663-110561846 | Common:5; Rare:65 | ||||
| chr13:111153451-111153720 | Common:3; Rare:118 | ||||
| chr13:113208633-113208751 | Rare:66 | ||||
| chr13:113490699-113490851 | Rare:51 | ||||
| chr13:113759140-113759297 | Common:1; Rare:44 | ||||
| chr13:114281519-114281654 | Common:2; Rare:75 | ||||
| chr14:20343199-20343669 | Common:12; Rare:282 | ||||
| chr14:20413420-20413528 | Common:2; Rare:30 | ||||
| chr14:20454754-20455287 | Common:7; Rare:140 | ||||
| chr14:20684471-20684608 | Common:1; Rare:20; Clinvar (benign):1 | ||||
| chr14:21456041-21456348 | Common:4; Rare:78 | ||||
| chr14:21476854-21477281 | Common:2; Rare:142 | ||||
| chr14:22589128-22589559 | Common:4; Rare:129 | ||||
| chr14:22766560-22766763 | Common:1; Rare:121 | ||||
| chr14:22766780-22766925 | Common:1; Rare:45 |