| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161314264-161314414 | Common:3; Rare:57; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr1:161749505-161749835 | Common:1; Rare:93 | ||||
| chr1:161750214-161750296 | Rare:26 | ||||
| chr1:161766163-161766366 | Common:3; Rare:60 | ||||
| chr1:162069601-162069717 | Common:1; Rare:32 | ||||
| chr1:162497707-162497867 | Common:2; Rare:51 | ||||
| chr1:162561336-162561627 | Common:3; Rare:110 | ||||
| chr1:162790516-162790831 | Common:4; Rare:95 | ||||
| chr1:163202895-163203255 | Common:1; Rare:67 | ||||
| chr1:163321693-163322208 | Common:1; Rare:134 | ||||
| chr1:164558647-164558724 | Rare:16 | ||||
| chr1:164558816-164559236 | Common:1; Rare:104 | ||||
| chr1:164559250-164559559 | Rare:75 | ||||
| chr1:164559591-164559756 | Common:2; Rare:33 | ||||
| chr1:165630784-165630886 | Rare:38 |