| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42456010-42456583 | Common:1; Rare:168 | ||||
| chr1:42456835-42456973 | Common:1; Rare:54; Clinvar (pathogenic):1 | ||||
| chr1:42658273-42658482 | Common:2; Rare:62 | ||||
| chr1:42682128-42682448 | Common:2; Rare:82 | ||||
| chr1:42682607-42682731 | Common:1; Rare:51 | ||||
| chr1:42683270-42683466 | Common:3; Rare:77 | ||||
| chr1:42766573-42766729 | Rare:40; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:42766983-42767309 | Common:4; Rare:109; Clinvar (benign):1 | ||||
| chr1:42817278-42817373 | Rare:42 | ||||
| chr1:42846387-42846642 | Common:1; Rare:75 | ||||
| chr1:42958849-42959042 | Common:1; Rare:50; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:43172214-43172330 | Common:1; Rare:57 | ||||
| chr1:43358662-43359011 | Common:7; Rare:111 | ||||
| chr1:43367957-43368241 | Rare:77 | ||||
| chr1:43389752-43389950 | Common:3; Rare:90 |