| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:156106404-156106804 | Common:15; Rare:398 | ||||
| chr1:156114030-156114430 | Common:4; Rare:67 | ||||
| chr1:156114435-156114835 | Common:2; Rare:381; Clinvar:20; Clinvar (benign):7 | ||||
| chr1:156115215-156115615 | Common:1; Rare:74; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr1:156122828-156123539 | Common:12; Rare:280 | ||||
| chr1:156123505-156123719 | Common:1; Rare:40 | ||||
| chr1:156126110-156126510 | Rare:197; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:156126430-156127309 | Common:7; Rare:211 | ||||
| chr1:156134810-156135190 | Common:2; Rare:88; Clinvar:14; Clinvar (benign):11; Clinvar (pathogenic):9 | ||||
| chr1:156135680-156136430 | Common:6; Rare:218; Clinvar:40; Clinvar (benign):26; Clinvar (pathogenic):15 | ||||
| chr1:156160830-156161270 | Common:3; Rare:298; Clinvar:6 | ||||
| chr1:156161290-156161953 | Common:7; Rare:349; Clinvar:3 | ||||
| chr1:156193706-156194226 | Common:18; Rare:550 | ||||
| chr1:156212664-156213068 | Common:6; Rare:340 | ||||
| chr1:156213006-156213595 | Common:15; Rare:918 |