| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:225818355-225818527 | Common:2; Rare:30 | ||||
| chr1:225826396-225826665 | Common:5; Rare:43 | ||||
| chr1:226703528-226703648 | Rare:41 | ||||
| chr1:226939127-226939487 | Common:4; Rare:60 | ||||
| chr1:226964998-226965716 | Common:5; Rare:236; Clinvar:9; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr1:226979007-226979294 | Common:1; Rare:61 | ||||
| chr1:226984547-226984941 | Common:3; Rare:143; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr1:228275993-228276142 | Common:1; Rare:46 | ||||
| chr1:228369156-228369449 | Common:1; Rare:61 | ||||
| chr1:228378371-228378742 | Common:2; Rare:156 | ||||
| chr1:231421014-231421175 | Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:234531152-234531377 | Common:2; Rare:36 | ||||
| chr1:234600055-234600304 | Common:7; Rare:104 | ||||
| chr1:234610176-234610320 | Common:2; Rare:58 | ||||
| chr1:234610871-234611210 | Common:4; Rare:126 |