| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:118088108-118088665 | Common:4; Rare:264 | ||||
| chr2:119223585-119223887 | Common:2; Rare:164 | ||||
| chr2:119366719-119367060 | Common:2; Rare:181 | ||||
| chr2:119367400-119367800 | Common:5; Rare:131 | ||||
| chr2:119431220-119431500 | Common:3; Rare:62 | ||||
| chr2:119431555-119431904 | Common:17; Rare:147 | ||||
| chr2:119679069-119679251 | Common:8; Rare:102 | ||||
| chr2:119759654-119760235 | Common:7; Rare:259 | ||||
| chr2:120012977-120013156 | Common:3; Rare:142 | ||||
| chr2:120013275-120013536 | Common:2; Rare:82 | ||||
| chr2:120223329-120223486 | Rare:91 | ||||
| chr2:120252591-120252969 | Common:6; Rare:242 | ||||
| chr2:121530240-121530520 | Common:3; Rare:133 | ||||
| chr2:121530547-121530906 | Common:15; Rare:300; Clinvar (pathogenic):4 | ||||
| chr2:121649108-121649711 | Common:5; Rare:251 |