| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:169107832-169107981 | Common:1; Rare:32 | ||||
| chr1:169367740-169368239 | Common:3; Rare:102 | ||||
| chr1:169485716-169485911 | Common:1; Rare:63; Clinvar:4; Clinvar (benign):4 | ||||
| chr1:169485941-169486169 | Rare:56; Clinvar:1 | ||||
| chr1:169794868-169795053 | Common:3; Rare:39 | ||||
| chr1:170074444-170074809 | Common:3; Rare:112 | ||||
| chr1:170532040-170532191 | Rare:66; Clinvar:1 | ||||
| chr1:171742030-171742191 | Common:1; Rare:49 | ||||
| chr1:171781371-171781682 | Common:3; Rare:77 | ||||
| chr1:171841366-171841546 | Common:3; Rare:57 | ||||
| chr1:173477002-173477488 | Common:5; Rare:163 | ||||
| chr1:173714879-173715029 | Common:1; Rare:36 | ||||
| chr1:173824402-173824708 | Rare:56; Clinvar:1 | ||||
| chr1:173867981-173868218 | Common:1; Rare:83 | ||||
| chr1:174159291-174159679 | Common:4; Rare:124 |