| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:99154933-99155037 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr2:99180977-99181233 | Common:2; Rare:73 | ||||
| chr2:99337243-99337466 | Rare:81 | ||||
| chr2:100417294-100417705 | Rare:116 | ||||
| chr2:100562855-100563050 | Common:3; Rare:64 | ||||
| chr2:101002162-101002577 | Rare:135 | ||||
| chr2:102736856-102736935 | Common:1; Rare:26 | ||||
| chr2:105037833-105038095 | Common:3; Rare:88 | ||||
| chr2:105337459-105337635 | Common:1; Rare:77 | ||||
| chr2:106887214-106887289 | Rare:19 | ||||
| chr2:108449108-108449268 | Rare:63 | ||||
| chr2:108719345-108719586 | Common:3; Rare:111; Clinvar (benign):2 | ||||
| chr2:109613865-109614008 | Common:2; Rare:50 | ||||
| chr2:111884156-111884246 | Rare:25 | ||||
| chr2:112255019-112255193 | Common:2; Rare:76 |