| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:155688604-155688839 | Common:1; Rare:64 | ||||
| chr1:155859338-155859588 | Common:3; Rare:60 | ||||
| chr1:155911285-155911505 | Common:1; Rare:86; Clinvar (benign):1 | ||||
| chr1:155934349-155934640 | Common:2; Rare:111 | ||||
| chr1:155978146-155978269 | Rare:31 | ||||
| chr1:155978468-155978667 | Common:1; Rare:57 | ||||
| chr1:156002464-156002791 | Common:1; Rare:35 | ||||
| chr1:156054615-156054897 | Common:3; Rare:80 | ||||
| chr1:156060982-156061211 | Common:1; Rare:59 | ||||
| chr1:156106356-156106727 | Common:3; Rare:70 | ||||
| chr1:156114539-156114842 | Common:1; Rare:67; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:156136042-156136388 | Common:3; Rare:118; Clinvar:19; Clinvar (benign):17; Clinvar (pathogenic):7 | ||||
| chr1:156193828-156194172 | Common:3; Rare:88 | ||||
| chr1:156212865-156213064 | Common:1; Rare:59 | ||||
| chr1:156282786-156282947 | Common:2; Rare:46 |