| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:13166892-13167165 | Common:5; Rare:56 | ||||
| chr2:15602967-15603268 | Common:1; Rare:72 | ||||
| chr2:15941664-15942138 | Common:1; Rare:131; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:16098447-16098689 | Rare:50 | ||||
| chr2:16794488-16794490 | |||||
| chr2:16795269-16795294 | Rare:4 | ||||
| chr2:17544009-17544163 | Rare:26 | ||||
| chr2:17595501-17595816 | Common:2; Rare:51 | ||||
| chr2:17722791-17723015 | Common:1; Rare:28 | ||||
| chr2:19228799-19229002 | Common:2; Rare:27 | ||||
| chr2:19348006-19348102 | Common:1; Rare:40 | ||||
| chr2:19985348-19985572 | Common:3; Rare:16 | ||||
| chr2:20082840-20083018 | Rare:32 | ||||
| chr2:24491236-24491293 | Common:1; Rare:24 | ||||
| chr2:25240312-25240727 | Common:1; Rare:159; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 |