| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96536569-96536773 | Common:1; Rare:55 | ||||
| chr2:97645880-97646147 | Common:3; Rare:80 | ||||
| chr2:97663993-97664251 | Rare:75 | ||||
| chr2:97713428-97713582 | Rare:20 | ||||
| chr2:98608440-98608629 | Common:1; Rare:83 | ||||
| chr2:99154884-99155101 | Common:2; Rare:87; Clinvar (benign):3 | ||||
| chr2:99180858-99181226 | Common:2; Rare:122 | ||||
| chr2:99337319-99337562 | Rare:94 | ||||
| chr2:100562640-100563054 | Common:5; Rare:122 | ||||
| chr2:101002042-101002316 | Rare:90 | ||||
| chr2:102736840-102736958 | Common:1; Rare:54 | ||||
| chr2:105038018-105038184 | Common:1; Rare:68 | ||||
| chr2:105337223-105337578 | Common:5; Rare:118 | ||||
| chr2:108534198-108534472 | Common:7; Rare:113 | ||||
| chr2:108719362-108719482 | Common:1; Rare:50 |