| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:119367140-119367460 | Common:1; Rare:68 | ||||
| chr2:119431704-119431931 | Common:4; Rare:60 | ||||
| chr2:119679102-119679225 | Common:3; Rare:37 | ||||
| chr2:119759692-119759928 | Common:1; Rare:66 | ||||
| chr2:120012937-120013091 | Common:2; Rare:67 | ||||
| chr2:120252608-120252978 | Common:3; Rare:120 | ||||
| chr2:121285092-121285349 | Common:2; Rare:97 | ||||
| chr2:121530579-121530895 | Common:7; Rare:142; Clinvar (pathogenic):2 | ||||
| chr2:121649399-121649702 | Common:2; Rare:89 | ||||
| chr2:121736744-121737098 | Common:4; Rare:144 | ||||
| chr2:121755433-121755759 | Common:4; Rare:107 | ||||
| chr2:127294077-127294235 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387897-127388255 | Common:9; Rare:158 | ||||
| chr2:127526404-127526607 | Common:2; Rare:75 | ||||
| chr2:127535536-127535814 | Common:1; Rare:48 |