| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42765920-42766160 | Common:8; Rare:44 | ||||
| chr1:42924241-42924478 | Common:1; Rare:76 | ||||
| chr1:42961367-42961524 | Common:1; Rare:21 | ||||
| chr1:42962619-42963019 | Common:3; Rare:115 | ||||
| chr1:42973196-42973596 | Common:3; Rare:84 | ||||
| chr1:43006055-43006159 | Rare:20 | ||||
| chr1:43006200-43006715 | Common:5; Rare:143 | ||||
| chr1:43007510-43007752 | Common:4; Rare:59 | ||||
| chr1:43008453-43008592 | Rare:28 | ||||
| chr1:43008745-43009313 | Common:2; Rare:166 | ||||
| chr1:43028330-43028730 | Common:1; Rare:124 | ||||
| chr1:43206779-43207253 | Common:2; Rare:189 | ||||
| chr1:43348920-43349300 | Common:2; Rare:131; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:43436320-43436680 | Common:1; Rare:63 | ||||
| chr1:43494150-43494500 | Common:1; Rare:53 |