| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:226062000-226062094 | Common:1; Rare:31 | ||||
| chr1:226062462-226062807 | Rare:124 | ||||
| chr1:226939991-226940388 | Rare:138; Clinvar:3 | ||||
| chr1:227735237-227735465 | Common:3; Rare:134 | ||||
| chr1:228103317-228103477 | Common:1; Rare:52 | ||||
| chr1:228109247-228109438 | Rare:59 | ||||
| chr1:228139856-228140094 | Common:1; Rare:57 | ||||
| chr1:228457865-228458132 | Common:1; Rare:95 | ||||
| chr1:229271027-229271331 | Rare:102 | ||||
| chr1:229434004-229434114 | Common:2; Rare:30; Clinvar (benign):2 | ||||
| chr1:230642454-230642543 | Common:1; Rare:39 | ||||
| chr1:230978739-230979108 | Common:2; Rare:139 | ||||
| chr1:231241101-231241362 | Common:2; Rare:129; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:231528495-231528723 | Common:2; Rare:77 | ||||
| chr1:234373387-234373594 | Common:1; Rare:103; Clinvar (benign):4 |