| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:205061715-205061848 | Common:1; Rare:26 | ||||
| chr1:205121882-205122593 | Common:6; Rare:191 | ||||
| chr1:205211177-205211485 | Common:1; Rare:126; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr1:205211518-205211770 | Rare:71 | ||||
| chr1:205227705-205227992 | Common:1; Rare:92 | ||||
| chr1:205321725-205321938 | Common:2; Rare:74 | ||||
| chr1:205456548-205456569 | Rare:5 | ||||
| chr1:205631325-205631781 | Common:5; Rare:155 | ||||
| chr1:205631788-205632266 | Common:4; Rare:160 | ||||
| chr1:205679864-205679998 | Rare:34 | ||||
| chr1:205680120-205680212 | Common:1; Rare:22 | ||||
| chr1:205680477-205680653 | Common:2; Rare:49 | ||||
| chr1:205749348-205749859 | Common:8; Rare:207 | ||||
| chr1:205749861-205750074 | Common:4; Rare:90 | ||||
| chr1:205750084-205750510 | Common:3; Rare:105 |