| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:230642210-230642593 | Common:2; Rare:190 | ||||
| chr1:230714074-230714601 | Common:10; Rare:207; Clinvar:18; Clinvar (benign):8 | ||||
| chr1:230868642-230869287 | Common:8; Rare:201 | ||||
| chr1:230978819-230979141 | Common:2; Rare:223 | ||||
| chr1:231241088-231241383 | Common:4; Rare:283; Clinvar:10; Clinvar (benign):4 | ||||
| chr1:231337795-231338096 | Common:6; Rare:197 | ||||
| chr1:231528504-231528760 | Common:4; Rare:167 | ||||
| chr1:231626641-231626845 | Common:2; Rare:58 | ||||
| chr1:232950436-232950721 | Common:7; Rare:170 | ||||
| chr1:234373288-234373835 | Common:4; Rare:448; Clinvar (benign):17 | ||||
| chr1:234478670-234479060 | Common:7; Rare:230 | ||||
| chr1:234479090-234479235 | Common:10; Rare:106 | ||||
| chr1:234608021-234608493 | Common:3; Rare:261 | ||||
| chr1:235128630-235129112 | Common:2; Rare:322 | ||||
| chr1:235161007-235161891 | Common:5; Rare:587 |