| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:65227591-65227877 | Rare:82 | ||||
| chr2:66434816-66435367 | Common:2; Rare:136 | ||||
| chr2:66435703-66435840 | Common:2; Rare:21 | ||||
| chr2:66439166-66439337 | Common:1; Rare:34 | ||||
| chr2:68157460-68157937 | Common:2; Rare:246 | ||||
| chr2:68252486-68252831 | Common:3; Rare:109 | ||||
| chr2:68467292-68467599 | Common:1; Rare:74 | ||||
| chr2:69387207-69387398 | Rare:53; Clinvar:2 | ||||
| chr2:69643622-69643825 | Rare:73 | ||||
| chr2:69829517-69829737 | Common:1; Rare:87 | ||||
| chr2:70086931-70087112 | Common:1; Rare:92 | ||||
| chr2:70087533-70087841 | Rare:107 | ||||
| chr2:71068526-71068654 | Rare:64 | ||||
| chr2:71130219-71130666 | Common:6; Rare:125; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73071701-73071848 | Common:2; Rare:57 |