| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:101002162-101002804 | Rare:189 | ||||
| chr2:101252794-101252886 | Common:2; Rare:36 | ||||
| chr2:101273042-101273113 | Rare:23 | ||||
| chr2:102736817-102736955 | Common:1; Rare:70 | ||||
| chr2:105037894-105038169 | Common:4; Rare:99 | ||||
| chr2:105337208-105337616 | Common:5; Rare:142 | ||||
| chr2:106194206-106194543 | Common:6; Rare:144 | ||||
| chr2:106887078-106887308 | Rare:66 | ||||
| chr2:106887493-106887549 | Common:1; Rare:7 | ||||
| chr2:107986383-107986600 | Common:1; Rare:47 | ||||
| chr2:108449102-108449277 | Rare:70 | ||||
| chr2:108719365-108719662 | Common:3; Rare:127; Clinvar (benign):2 | ||||
| chr2:108786638-108786846 | Common:6; Rare:117 | ||||
| chr2:109613871-109614008 | Common:2; Rare:46 | ||||
| chr2:110204913-110205054 | Common:1; Rare:63; Clinvar:3; Clinvar (benign):1 |