| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112645688-112645951 | Common:1; Rare:97 | ||||
| chr2:112764575-112764803 | Common:2; Rare:76; Clinvar (pathogenic):1 | ||||
| chr2:113278919-113279106 | Common:1; Rare:40 | ||||
| chr2:113627041-113627266 | Common:1; Rare:65 | ||||
| chr2:113889765-113890180 | Common:8; Rare:130 | ||||
| chr2:118014056-118014221 | Common:2; Rare:93 | ||||
| chr2:119366795-119367087 | Common:1; Rare:89 | ||||
| chr2:119679102-119679219 | Common:3; Rare:33 | ||||
| chr2:120252608-120252964 | Common:3; Rare:117 | ||||
| chr2:121285194-121285337 | Rare:48 | ||||
| chr2:121530609-121530880 | Common:7; Rare:109 | ||||
| chr2:121649431-121649650 | Common:2; Rare:65 | ||||
| chr2:121736846-121737229 | Common:5; Rare:143 | ||||
| chr2:127294094-127294212 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127811121-127811285 | Common:1; Rare:58 |