| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:7954052-7954290 | Rare:62 | ||||
| chr1:7961457-7961778 | Common:4; Rare:108; Clinvar:2; Clinvar (benign):3 | ||||
| chr1:8026281-8026500 | Common:2; Rare:101 | ||||
| chr1:8423631-8423913 | Common:1; Rare:119 | ||||
| chr1:8878578-8878835 | Rare:130 | ||||
| chr1:9239771-9239993 | Common:2; Rare:50 | ||||
| chr1:9942782-9942951 | Common:1; Rare:30 | ||||
| chr1:9943063-9943504 | Common:6; Rare:115 | ||||
| chr1:10032687-10033002 | Common:2; Rare:87 | ||||
| chr1:10210339-10210593 | Common:4; Rare:67 | ||||
| chr1:10398784-10399125 | Common:2; Rare:135 | ||||
| chr1:10474847-10474988 | Rare:45; Clinvar:2 | ||||
| chr1:11012620-11012734 | Common:1; Rare:38; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:11099814-11099921 | Common:1; Rare:44 | ||||
| chr1:11262495-11262850 | Common:2; Rare:104 |