| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:6208680-6208866 | Common:1; Rare:51 | ||||
| chr1:7961431-7961758 | Common:4; Rare:119; Clinvar:2; Clinvar (benign):3 | ||||
| chr1:8026169-8026459 | Common:2; Rare:131 | ||||
| chr1:8878585-8878835 | Rare:127 | ||||
| chr1:9943318-9943488 | Common:2; Rare:38 | ||||
| chr1:10032763-10032965 | Rare:53 | ||||
| chr1:10398837-10399118 | Common:2; Rare:112 | ||||
| chr1:11055068-11055114 | Common:2; Rare:15 | ||||
| chr1:11099784-11099957 | Common:2; Rare:71 | ||||
| chr1:11262506-11262828 | Common:2; Rare:95 | ||||
| chr1:11654821-11654951 | Common:2; Rare:29 | ||||
| chr1:11691477-11691781 | Common:4; Rare:72 | ||||
| chr1:11805939-11806265 | Common:2; Rare:85 | ||||
| chr1:11934512-11934754 | Common:3; Rare:79; Clinvar:5; Clinvar (benign):1 | ||||
| chr1:11980089-11980462 | Common:6; Rare:119; Clinvar:1; Clinvar (benign):4 |