| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:92080228-92080572 | Common:3; Rare:85 | ||||
| chr1:92298945-92299076 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:92784615-92784883 | Common:2; Rare:75 | ||||
| chr1:92961426-92961809 | Common:3; Rare:116 | ||||
| chr1:93079097-93079308 | Common:2; Rare:88 | ||||
| chr1:93179840-93179961 | Common:1; Rare:27 | ||||
| chr1:93180047-93180738 | Common:1; Rare:268 | ||||
| chr1:93345754-93345953 | Common:4; Rare:78 | ||||
| chr1:93448002-93448182 | Common:2; Rare:66 | ||||
| chr1:93847211-93847273 | Common:1; Rare:15 | ||||
| chr1:93879099-93879274 | Common:1; Rare:67 | ||||
| chr1:94418175-94418480 | Common:2; Rare:112 | ||||
| chr1:94541730-94541998 | Rare:78 | ||||
| chr1:94820154-94820557 | Common:6; Rare:108 | ||||
| chr1:94903120-94903526 | Common:1; Rare:82 |