| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42456886-42456963 | Rare:33 | ||||
| chr1:42462999-42463352 | Common:4; Rare:113 | ||||
| chr1:42657978-42658091 | Rare:24 | ||||
| chr1:42658238-42658522 | Common:2; Rare:84 | ||||
| chr1:42682031-42682439 | Common:2; Rare:122 | ||||
| chr1:42682961-42683062 | Common:1; Rare:40 | ||||
| chr1:42683064-42683246 | Rare:98 | ||||
| chr1:42740225-42740415 | Common:1; Rare:41 | ||||
| chr1:42766960-42767393 | Common:7; Rare:154; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:42767406-42767627 | Rare:77 | ||||
| chr1:42816923-42817158 | Common:1; Rare:71 | ||||
| chr1:42817185-42817422 | Rare:93 | ||||
| chr1:42846342-42846743 | Common:1; Rare:113 | ||||
| chr1:42957993-42958391 | Common:7; Rare:128 | ||||
| chr1:42958734-42959259 | Common:6; Rare:127; Clinvar:8; Clinvar (benign):5 |