| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:101252658-101252917 | Common:5; Rare:87 | ||||
| chr2:101252983-101253222 | Common:2; Rare:76 | ||||
| chr2:101308606-101308840 | Common:1; Rare:111 | ||||
| chr2:102141638-102141840 | Common:1; Rare:34 | ||||
| chr2:102142631-102142909 | Common:3; Rare:85 | ||||
| chr2:102355668-102355850 | Common:2; Rare:48 | ||||
| chr2:102736799-102736955 | Common:1; Rare:80 | ||||
| chr2:105037875-105038148 | Common:4; Rare:99 | ||||
| chr2:105337435-105337626 | Common:3; Rare:88 | ||||
| chr2:106194210-106194568 | Common:6; Rare:154 | ||||
| chr2:108449036-108449257 | Rare:82 | ||||
| chr2:108534186-108534504 | Common:7; Rare:127 | ||||
| chr2:108719383-108719598 | Common:3; Rare:90; Clinvar (benign):2 | ||||
| chr2:109613823-109614008 | Common:2; Rare:65 | ||||
| chr2:109614153-109614364 | Common:2; Rare:71 |