| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:118013968-118014215 | Common:3; Rare:128 | ||||
| chr2:118088356-118088523 | Common:1; Rare:51 | ||||
| chr2:119366789-119367049 | Common:1; Rare:77 | ||||
| chr2:119759791-119759954 | Common:1; Rare:52 | ||||
| chr2:121530559-121530884 | Common:7; Rare:135 | ||||
| chr2:121649415-121649656 | Common:2; Rare:69 | ||||
| chr2:121650011-121650151 | Rare:37 | ||||
| chr2:121736833-121737116 | Common:5; Rare:107 | ||||
| chr2:127107276-127107477 | Common:4; Rare:49; Clinvar (benign):1 | ||||
| chr2:127294079-127294231 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387953-127388219 | Common:4; Rare:116 | ||||
| chr2:127811150-127811239 | Rare:26 | ||||
| chr2:127858090-127858211 | Common:1; Rare:66 | ||||
| chr2:127885954-127885961 | Rare:2 | ||||
| chr2:130181538-130181700 | Common:2; Rare:57 |