| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:160205204-160205520 | Common:2; Rare:84 | ||||
| chr1:160219150-160219305 | Rare:29 | ||||
| chr1:160261638-160261734 | Common:1; Rare:23 | ||||
| chr1:160262432-160262743 | Common:2; Rare:94 | ||||
| chr1:160343133-160343467 | Rare:129 | ||||
| chr1:161038724-161039072 | Common:4; Rare:107 | ||||
| chr1:161045866-161046057 | Common:1; Rare:49 | ||||
| chr1:161117953-161118141 | Rare:92 | ||||
| chr1:161118184-161118334 | Common:1; Rare:45 | ||||
| chr1:161132417-161132679 | Common:1; Rare:91 | ||||
| chr1:161159293-161159526 | Common:2; Rare:63 | ||||
| chr1:161166268-161166532 | Common:3; Rare:63; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:161197188-161197470 | Common:3; Rare:47 | ||||
| chr1:161199048-161199156 | Rare:22 | ||||
| chr1:161209478-161210395 | Common:3; Rare:222; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 |