| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44739626-44739897 | Common:2; Rare:108 | ||||
| chr1:44775438-44775599 | Common:1; Rare:64 | ||||
| chr1:44775758-44776140 | Common:2; Rare:138 | ||||
| chr1:44777615-44778143 | Common:2; Rare:131 | ||||
| chr1:45339938-45340232 | Common:1; Rare:110; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr1:45340381-45340470 | Common:1; Rare:24; Clinvar:1 | ||||
| chr1:45500040-45500369 | Common:1; Rare:81; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr1:45521827-45521972 | Common:1; Rare:60 | ||||
| chr1:45550741-45551086 | Common:3; Rare:83 | ||||
| chr1:45686466-45686651 | Rare:65 | ||||
| chr1:45687054-45687353 | Common:1; Rare:80 | ||||
| chr1:45688055-45688216 | Common:1; Rare:41 | ||||
| chr1:45750606-45750839 | Rare:83 | ||||
| chr1:46133037-46133232 | Common:2; Rare:49 | ||||
| chr1:46198389-46198522 | Common:1; Rare:54; Clinvar:1 |