| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:9943290-9943488 | Common:2; Rare:48 | ||||
| chr1:10032763-10033025 | Common:1; Rare:70 | ||||
| chr1:10398734-10399114 | Common:2; Rare:140 | ||||
| chr1:10430244-10430486 | Common:5; Rare:62 | ||||
| chr1:10472461-10472696 | Rare:52 | ||||
| chr1:11099740-11099922 | Common:2; Rare:77 | ||||
| chr1:11262493-11262821 | Common:2; Rare:100 | ||||
| chr1:11654417-11654501 | Rare:24 | ||||
| chr1:11654811-11654938 | Common:2; Rare:35 | ||||
| chr1:11680601-11680692 | Common:1; Rare:23 | ||||
| chr1:11691453-11691763 | Common:4; Rare:68 | ||||
| chr1:11691771-11691835 | Rare:9 | ||||
| chr1:11692043-11692082 | Rare:7 | ||||
| chr1:11805935-11806265 | Common:2; Rare:89; Clinvar:1 | ||||
| chr1:11934619-11934754 | Common:2; Rare:50; Clinvar:5; Clinvar (benign):1 |