| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161117951-161118141 | Rare:92 | ||||
| chr1:161132426-161132726 | Common:1; Rare:100 | ||||
| chr1:161133091-161133164 | Rare:14 | ||||
| chr1:161159392-161159544 | Common:1; Rare:47 | ||||
| chr1:161160429-161160707 | Rare:61 | ||||
| chr1:161166263-161166512 | Common:2; Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:161225768-161226069 | Common:10; Rare:44 | ||||
| chr1:161258633-161258749 | Common:1; Rare:23 | ||||
| chr1:161314262-161314443 | Common:4; Rare:74; Clinvar:10; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr1:161367857-161367905 | Rare:10 | ||||
| chr1:161749749-161749835 | Rare:36 | ||||
| chr1:161749858-161749874 | Rare:9 | ||||
| chr1:161750178-161750212 | Rare:8 | ||||
| chr1:161750214-161750300 | Rare:27 | ||||
| chr1:161766225-161766540 | Common:5; Rare:98; Clinvar (pathogenic):1 |