| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:9877939-9878026 | Rare:13 | ||||
| chr1:9943284-9943488 | Common:2; Rare:51 | ||||
| chr1:10398716-10399125 | Common:2; Rare:149 | ||||
| chr1:11072090-11072357 | Common:1; Rare:52 | ||||
| chr1:11099722-11100015 | Common:3; Rare:111 | ||||
| chr1:11189153-11189355 | Common:1; Rare:42 | ||||
| chr1:11262490-11262810 | Common:2; Rare:98 | ||||
| chr1:11654380-11654558 | Rare:44 | ||||
| chr1:11654705-11654930 | Common:4; Rare:60 | ||||
| chr1:11736026-11736206 | Common:3; Rare:56 | ||||
| chr1:11805469-11805609 | Common:2; Rare:24 | ||||
| chr1:11805858-11806265 | Common:2; Rare:115; Clinvar:2 | ||||
| chr1:11979958-11980339 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:12229707-12230113 | Common:3; Rare:114 | ||||
| chr1:12616619-12616837 | Common:1; Rare:42 |