| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:101252650-101252907 | Common:5; Rare:86 | ||||
| chr2:101308675-101308806 | Rare:50 | ||||
| chr2:101991661-101991977 | Common:1; Rare:76 | ||||
| chr2:102104349-102104393 | Common:1; Rare:7 | ||||
| chr2:102104529-102104718 | Common:4; Rare:51 | ||||
| chr2:102141663-102141881 | Common:1; Rare:41 | ||||
| chr2:102142670-102142998 | Common:5; Rare:103 | ||||
| chr2:102736856-102736921 | Common:1; Rare:22 | ||||
| chr2:105037894-105038148 | Common:4; Rare:91 | ||||
| chr2:105337436-105337606 | Common:3; Rare:84 | ||||
| chr2:106194237-106194568 | Common:6; Rare:140 | ||||
| chr2:108534204-108534534 | Common:8; Rare:134 | ||||
| chr2:108719345-108719586 | Common:3; Rare:111; Clinvar (benign):2 | ||||
| chr2:109613798-109614008 | Common:3; Rare:73 | ||||
| chr2:111122436-111122723 | Common:3; Rare:123 |