| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:263993-264171 | Common:2; Rare:54 | ||||
| chr2:264494-264967 | Common:4; Rare:173 | ||||
| chr2:677352-677528 | Common:1; Rare:70 | ||||
| chr2:3379625-3379761 | Common:1; Rare:54 | ||||
| chr2:3519492-3519582 | Common:2; Rare:35 | ||||
| chr2:3558251-3558481 | Common:5; Rare:101 | ||||
| chr2:3575107-3575358 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423169-9423683 | Common:1; Rare:141 | ||||
| chr2:9474463-9474570 | Common:7; Rare:45 | ||||
| chr2:9555669-9555966 | Common:2; Rare:101 | ||||
| chr2:9843411-9843533 | Common:3; Rare:33 | ||||
| chr2:10689902-10690024 | Common:2; Rare:47 | ||||
| chr2:11746364-11746671 | Common:2; Rare:86; Clinvar:4 | ||||
| chr2:12716756-12717053 | Common:1; Rare:86 | ||||
| chr2:17753737-17753866 | Common:1; Rare:48 |