| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:51878510-51878584 | Common:1; Rare:31 | ||||
| chr1:51878586-51879013 | Common:1; Rare:123 | ||||
| chr1:52055084-52055264 | Common:1; Rare:51 | ||||
| chr1:52056129-52056359 | Rare:66 | ||||
| chr1:52141886-52142274 | Rare:102 | ||||
| chr1:52366086-52366301 | Common:1; Rare:64 | ||||
| chr1:52404460-52404767 | Common:2; Rare:97 | ||||
| chr1:52552827-52552961 | Common:1; Rare:40 | ||||
| chr1:52553039-52553375 | Common:4; Rare:99 | ||||
| chr1:52553442-52553697 | Common:3; Rare:73 | ||||
| chr1:52553820-52553872 | Rare:18 | ||||
| chr1:52602113-52602506 | Common:3; Rare:100 | ||||
| chr1:52698318-52698460 | Common:2; Rare:50 | ||||
| chr1:52927188-52927371 | Common:4; Rare:60 | ||||
| chr1:53196553-53196832 | Common:1; Rare:76; Clinvar:5; Clinvar (benign):1 |