| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:118014037-118014249 | Common:2; Rare:115 | ||||
| chr2:118088302-118088526 | Common:1; Rare:66 | ||||
| chr2:119366580-119367076 | Common:4; Rare:126 | ||||
| chr2:119367140-119367476 | Common:1; Rare:74 | ||||
| chr2:119678956-119679234 | Common:6; Rare:74 | ||||
| chr2:119759700-119759878 | Common:1; Rare:51 | ||||
| chr2:121530324-121530889 | Common:10; Rare:205; Clinvar (pathogenic):1 | ||||
| chr2:121649404-121649654 | Common:2; Rare:73 | ||||
| chr2:121649892-121650138 | Common:1; Rare:64 | ||||
| chr2:121736736-121737118 | Common:5; Rare:157 | ||||
| chr2:121755415-121755838 | Common:5; Rare:138 | ||||
| chr2:124025124-124025320 | Common:2; Rare:66 | ||||
| chr2:127294077-127294219 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387904-127388255 | Common:9; Rare:156 | ||||
| chr2:127526425-127526596 | Common:2; Rare:55 |