| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9474491-9474630 | Common:6; Rare:63 | ||||
| chr2:9555621-9556029 | Common:2; Rare:136 | ||||
| chr2:9630944-9631168 | Common:2; Rare:77 | ||||
| chr2:9843124-9843209 | Rare:24 | ||||
| chr2:9843250-9843553 | Common:6; Rare:90 | ||||
| chr2:9843597-9843932 | Common:4; Rare:91 | ||||
| chr2:10689910-10690006 | Common:2; Rare:33 | ||||
| chr2:11465844-11466184 | Common:3; Rare:107 | ||||
| chr2:11746475-11746674 | Common:2; Rare:64; Clinvar:4 | ||||
| chr2:12716756-12717048 | Common:1; Rare:86 | ||||
| chr2:17539719-17539993 | Common:2; Rare:52 | ||||
| chr2:17540345-17540888 | Common:4; Rare:128 | ||||
| chr2:17753079-17753419 | Common:5; Rare:84 | ||||
| chr2:17753662-17754195 | Common:6; Rare:166; Clinvar (benign):1 | ||||
| chr2:18560240-18560397 | Common:1; Rare:56 |