| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:118014068-118014221 | Common:2; Rare:88 | ||||
| chr2:119366795-119367068 | Common:1; Rare:82 | ||||
| chr2:119431704-119431866 | Common:4; Rare:41 | ||||
| chr2:119678982-119679240 | Common:6; Rare:69 | ||||
| chr2:120012913-120013135 | Common:3; Rare:100 | ||||
| chr2:120252606-120252945 | Common:3; Rare:111 | ||||
| chr2:121285194-121285340 | Rare:50 | ||||
| chr2:121530580-121530880 | Common:7; Rare:120 | ||||
| chr2:121649427-121649645 | Common:2; Rare:64 | ||||
| chr2:121736723-121737242 | Common:5; Rare:208 | ||||
| chr2:121755415-121755770 | Common:5; Rare:119 | ||||
| chr2:127294077-127294243 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387962-127388255 | Common:7; Rare:128 | ||||
| chr2:127526363-127526588 | Common:2; Rare:86 | ||||
| chr2:127526803-127526945 | Rare:26 |