| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44739667-44739894 | Common:1; Rare:88 | ||||
| chr1:44775438-44775599 | Common:1; Rare:64 | ||||
| chr1:44775833-44776140 | Common:2; Rare:112 | ||||
| chr1:44777615-44778101 | Common:2; Rare:124 | ||||
| chr1:44986545-44986733 | Common:2; Rare:33; Clinvar (benign):1 | ||||
| chr1:45339957-45340193 | Rare:82 | ||||
| chr1:45340376-45340480 | Common:2; Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:45500046-45500358 | Common:1; Rare:76; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr1:45521827-45522013 | Common:1; Rare:75 | ||||
| chr1:45550709-45551076 | Common:3; Rare:94 | ||||
| chr1:45687059-45687318 | Common:1; Rare:70 | ||||
| chr1:45688059-45688211 | Common:1; Rare:39 | ||||
| chr1:45750621-45750817 | Rare:71 | ||||
| chr1:46132833-46133233 | Common:3; Rare:109 | ||||
| chr1:46198384-46198552 | Common:4; Rare:82; Clinvar:1 |