| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:10812680-10812971 | Common:3; Rare:115 | ||||
| chr2:11465773-11466191 | Common:4; Rare:141 | ||||
| chr2:11746369-11746655 | Common:1; Rare:77; Clinvar:2 | ||||
| chr2:12716608-12717062 | Common:4; Rare:141 | ||||
| chr2:12718075-12718238 | Common:1; Rare:31 | ||||
| chr2:14632509-14632784 | Rare:95 | ||||
| chr2:15940353-15940557 | Rare:50 | ||||
| chr2:16665798-16665951 | Common:4; Rare:33 | ||||
| chr2:17540436-17540714 | Common:1; Rare:66 | ||||
| chr2:17753096-17753408 | Common:4; Rare:82 | ||||
| chr2:17753686-17754175 | Common:5; Rare:152; Clinvar (benign):1 | ||||
| chr2:18560322-18560571 | Rare:97 | ||||
| chr2:18560663-18560801 | Rare:36 | ||||
| chr2:19901602-19901729 | Common:1; Rare:60 | ||||
| chr2:19901876-19902131 | Common:3; Rare:79 |