| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:101002156-101002322 | Rare:63 | ||||
| chr2:101252650-101252907 | Common:5; Rare:86 | ||||
| chr2:101308679-101308806 | Rare:48 | ||||
| chr2:101998823-101999021 | Common:1; Rare:18 | ||||
| chr2:102142667-102142829 | Rare:56 | ||||
| chr2:102187719-102187852 | Common:1; Rare:40 | ||||
| chr2:102736834-102736921 | Common:1; Rare:40 | ||||
| chr2:105337448-105337616 | Common:2; Rare:80 | ||||
| chr2:108449021-108449268 | Common:1; Rare:98 | ||||
| chr2:108534158-108534513 | Common:7; Rare:143 | ||||
| chr2:108719344-108719586 | Common:3; Rare:112; Clinvar (benign):2 | ||||
| chr2:109613803-109614043 | Common:2; Rare:82 | ||||
| chr2:109614112-109614364 | Common:4; Rare:89 | ||||
| chr2:110678032-110678202 | Rare:46 | ||||
| chr2:111122441-111122733 | Common:3; Rare:124 |