| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:230978833-230979099 | Common:1; Rare:94 | ||||
| chr1:231241071-231241352 | Common:2; Rare:135; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:231337803-231338049 | Common:2; Rare:91 | ||||
| chr1:231528591-231528758 | Common:1; Rare:59 | ||||
| chr1:234373620-234373766 | Rare:61; Clinvar (benign):3 | ||||
| chr1:234608166-234608390 | Rare:75 | ||||
| chr1:234609281-234609383 | Rare:26 | ||||
| chr1:235328116-235328614 | Common:4; Rare:153 | ||||
| chr1:235866842-235867177 | Common:3; Rare:103 | ||||
| chr1:236065156-236065267 | Common:1; Rare:45 | ||||
| chr1:236524512-236524599 | Common:1; Rare:18 | ||||
| chr1:243255055-243255148 | Rare:25 | ||||
| chr1:243255741-243256188 | Common:1; Rare:135; Clinvar:5; Clinvar (benign):1 | ||||
| chr1:244859273-244859507 | Rare:65; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr1:244863616-244864142 | Common:1; Rare:178; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):1 |