| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:19312051-19312346 | Common:8; Rare:144 | ||||
| chr1:19485434-19485746 | Common:1; Rare:107 | ||||
| chr1:19596919-19597261 | Common:3; Rare:134 | ||||
| chr1:20660918-20661285 | Common:3; Rare:120; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:20661323-20661682 | Common:3; Rare:133; Clinvar:4; Clinvar (benign):6 | ||||
| chr1:21345454-21345638 | Common:2; Rare:68 | ||||
| chr1:21440018-21440184 | Common:2; Rare:39 | ||||
| chr1:23019325-23019611 | Rare:104 | ||||
| chr1:23194792-23194961 | Common:1; Rare:39 | ||||
| chr1:23368865-23369010 | Common:1; Rare:49 | ||||
| chr1:23559400-23559654 | Common:1; Rare:111 | ||||
| chr1:23778225-23778507 | Common:9; Rare:139 | ||||
| chr1:23825357-23825539 | Common:3; Rare:62; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr1:24413678-24413799 | Common:1; Rare:32 | ||||
| chr1:24415633-24415875 | Common:1; Rare:61 |