| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:102423009-102423225 | Common:1; Rare:46 | ||||
| chr2:102736811-102736955 | Common:1; Rare:74 | ||||
| chr2:105037894-105038117 | Common:3; Rare:79 | ||||
| chr2:105329656-105329966 | Common:2; Rare:93 | ||||
| chr2:105337454-105337620 | Common:1; Rare:79 | ||||
| chr2:105398961-105399271 | Common:1; Rare:111 | ||||
| chr2:106194237-106194559 | Common:6; Rare:137 | ||||
| chr2:108449071-108449268 | Rare:82 | ||||
| chr2:108534186-108534502 | Common:7; Rare:127 | ||||
| chr2:108621129-108621302 | Rare:28 | ||||
| chr2:108719356-108719564 | Common:3; Rare:87; Clinvar (benign):1 | ||||
| chr2:109613846-109614047 | Common:2; Rare:74 | ||||
| chr2:110678001-110678258 | Rare:86 | ||||
| chr2:111120754-111121080 | Common:6; Rare:137 | ||||
| chr2:111122436-111122733 | Common:3; Rare:125 |