| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113756482-113756791 | Common:4; Rare:100 | ||||
| chr2:113889766-113890322 | Common:9; Rare:168 | ||||
| chr2:118014006-118014275 | Common:3; Rare:139 | ||||
| chr2:118088337-118088523 | Common:1; Rare:56 | ||||
| chr2:118847646-118847889 | Common:8; Rare:80 | ||||
| chr2:119366742-119367072 | Common:1; Rare:101 | ||||
| chr2:119431596-119431906 | Common:9; Rare:76 | ||||
| chr2:119679089-119679225 | Common:3; Rare:45 | ||||
| chr2:120252618-120252973 | Common:3; Rare:117 | ||||
| chr2:121530583-121530884 | Common:7; Rare:124 | ||||
| chr2:121649375-121649816 | Common:3; Rare:125 | ||||
| chr2:121649927-121650133 | Rare:58 | ||||
| chr2:121736828-121737229 | Common:5; Rare:154 | ||||
| chr2:121755410-121755821 | Common:5; Rare:135 | ||||
| chr2:127294077-127294214 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):2 |