| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113889761-113890165 | Common:8; Rare:130 | ||||
| chr2:118014007-118014190 | Common:2; Rare:109 | ||||
| chr2:118088167-118088521 | Common:2; Rare:95 | ||||
| chr2:119366779-119367065 | Common:1; Rare:86 | ||||
| chr2:119679072-119679212 | Common:3; Rare:45 | ||||
| chr2:120252603-120252973 | Common:3; Rare:122 | ||||
| chr2:121285182-121285319 | Rare:47 | ||||
| chr2:121530279-121530439 | Rare:45 | ||||
| chr2:121530596-121530889 | Common:7; Rare:124; Clinvar (pathogenic):1 | ||||
| chr2:121649418-121649645 | Common:2; Rare:65 | ||||
| chr2:127294077-127294243 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127526293-127526607 | Common:2; Rare:115 | ||||
| chr2:127675072-127675373 | Common:3; Rare:45 | ||||
| chr2:127885864-127886272 | Common:1; Rare:111 | ||||
| chr2:128091058-128091335 | Common:8; Rare:93 |