| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113889703-113890285 | Common:9; Rare:186 | ||||
| chr2:113891013-113891128 | Rare:27 | ||||
| chr2:118014007-118014243 | Common:2; Rare:124 | ||||
| chr2:118088319-118088535 | Common:1; Rare:62 | ||||
| chr2:119223665-119223840 | Common:1; Rare:51 | ||||
| chr2:119366749-119367070 | Common:1; Rare:100 | ||||
| chr2:119367571-119367711 | Rare:46 | ||||
| chr2:119678951-119679225 | Common:5; Rare:75 | ||||
| chr2:120012937-120013155 | Common:3; Rare:103 | ||||
| chr2:120252606-120252964 | Common:3; Rare:118 | ||||
| chr2:121530579-121530889 | Common:7; Rare:132; Clinvar (pathogenic):1 | ||||
| chr2:121649394-121649748 | Common:2; Rare:107 | ||||
| chr2:121650047-121650163 | Rare:30 | ||||
| chr2:121736716-121737261 | Common:5; Rare:219 | ||||
| chr2:121755437-121755792 | Common:5; Rare:116 |