| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:101002162-101002318 | Rare:61 | ||||
| chr2:101252658-101252907 | Common:5; Rare:82 | ||||
| chr2:101273042-101273110 | Rare:21 | ||||
| chr2:101308680-101308806 | Rare:48 | ||||
| chr2:101991781-101991982 | Common:1; Rare:53 | ||||
| chr2:102142609-102142960 | Common:5; Rare:101 | ||||
| chr2:102736806-102736932 | Common:1; Rare:67 | ||||
| chr2:105037884-105038156 | Common:4; Rare:99 | ||||
| chr2:105337468-105337610 | Common:1; Rare:70 | ||||
| chr2:106194237-106194554 | Common:6; Rare:135 | ||||
| chr2:108377853-108377993 | Rare:30 | ||||
| chr2:108449097-108449260 | Rare:58 | ||||
| chr2:108534204-108534534 | Common:8; Rare:134 | ||||
| chr2:108588130-108588428 | Common:2; Rare:50 | ||||
| chr2:108719372-108719625 | Common:3; Rare:104; Clinvar (benign):2 |