| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113889766-113890183 | Common:8; Rare:129 | ||||
| chr2:118014037-118014193 | Common:2; Rare:98 | ||||
| chr2:118088344-118088529 | Common:1; Rare:54 | ||||
| chr2:119366798-119367080 | Common:1; Rare:85 | ||||
| chr2:119431653-119431862 | Common:6; Rare:53 | ||||
| chr2:119678995-119679214 | Common:4; Rare:61 | ||||
| chr2:120252591-120252967 | Common:3; Rare:122 | ||||
| chr2:121530579-121530880 | Common:7; Rare:121 | ||||
| chr2:121649404-121649659 | Common:2; Rare:74 | ||||
| chr2:121736760-121737094 | Common:4; Rare:133 | ||||
| chr2:127294088-127294212 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127526395-127526619 | Common:2; Rare:84 | ||||
| chr2:127650529-127650687 | Common:5; Rare:38 | ||||
| chr2:127858112-127858326 | Common:3; Rare:79 | ||||
| chr2:127885849-127885979 | Rare:30 |