| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113889747-113890314 | Common:9; Rare:175 | ||||
| chr2:118014023-118014221 | Common:2; Rare:109 | ||||
| chr2:118088302-118088529 | Common:1; Rare:66 | ||||
| chr2:119366749-119367059 | Common:1; Rare:94 | ||||
| chr2:119679086-119679236 | Common:4; Rare:48 | ||||
| chr2:119759718-119759831 | Common:1; Rare:28 | ||||
| chr2:120012985-120013121 | Common:1; Rare:67 | ||||
| chr2:121490286-121490487 | Rare:42 | ||||
| chr2:121530373-121530884 | Common:10; Rare:182 | ||||
| chr2:121649415-121649654 | Common:2; Rare:68 | ||||
| chr2:121736736-121737105 | Common:4; Rare:149 | ||||
| chr2:121755392-121755792 | Common:6; Rare:130 | ||||
| chr2:124025166-124025320 | Common:2; Rare:53 | ||||
| chr2:127294077-127294219 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387928-127388217 | Common:6; Rare:127 |