| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:160262444-160262669 | Common:1; Rare:72 | ||||
| chr1:160343171-160343461 | Rare:121 | ||||
| chr1:160862661-160862716 | Rare:21 | ||||
| chr1:160862718-160862947 | Common:2; Rare:38 | ||||
| chr1:161021130-161021314 | Rare:47 | ||||
| chr1:161038899-161039072 | Common:2; Rare:56 | ||||
| chr1:161045878-161046064 | Common:1; Rare:48 | ||||
| chr1:161069862-161070145 | Rare:35 | ||||
| chr1:161117956-161118149 | Rare:98 | ||||
| chr1:161132426-161132647 | Common:1; Rare:78 | ||||
| chr1:161159366-161159520 | Common:2; Rare:41 | ||||
| chr1:161166268-161166521 | Common:2; Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:161209681-161209906 | Rare:46; Clinvar (benign):1 | ||||
| chr1:161306143-161306322 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:161314268-161314434 | Common:3; Rare:67; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):1 |