| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:151619387-151619494 | Common:2; Rare:33; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:151637239-151637425 | Rare:35 | ||||
| chr2:151637606-151637665 | Rare:9 | ||||
| chr2:152200652-152200874 | Rare:40 | ||||
| chr2:152251923-152251975 | Rare:11 | ||||
| chr2:152335975-152336051 | Common:1; Rare:15 | ||||
| chr2:152336225-152336280 | Rare:14 | ||||
| chr2:152336668-152336693 | Rare:4 | ||||
| chr2:152407398-152407537 | Rare:25 | ||||
| chr2:152421451-152421594 | Rare:28 | ||||
| chr2:152421603-152421753 | Rare:26 | ||||
| chr2:152432223-152432537 | Common:1; Rare:60 | ||||
| chr2:152537379-152537520 | Common:3; Rare:30 | ||||
| chr2:152573468-152573472 | Common:1 | ||||
| chr2:156333883-156333983 | Common:1; Rare:21 |