| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:9687338-9687705 | Common:2; Rare:90 | ||||
| chr1:9823793-9824223 | Common:3; Rare:134 | ||||
| chr1:9910113-9910810 | Common:7; Rare:225 | ||||
| chr1:9942545-9942650 | Rare:36 | ||||
| chr1:9942886-9942962 | Rare:16 | ||||
| chr1:9942996-9943595 | Common:7; Rare:160 | ||||
| chr1:10032517-10033048 | Common:4; Rare:141 | ||||
| chr1:10033362-10033513 | Common:2; Rare:23 | ||||
| chr1:10210253-10210649 | Common:6; Rare:116 | ||||
| chr1:10398450-10398593 | Common:3; Rare:32 | ||||
| chr1:10398777-10399145 | Common:2; Rare:139 | ||||
| chr1:10430339-10430527 | Common:3; Rare:56 | ||||
| chr1:10430578-10430835 | Common:6; Rare:90 | ||||
| chr1:10472365-10472839 | Rare:121 | ||||
| chr1:10474786-10475273 | Common:1; Rare:151; Clinvar:4; Clinvar (benign):1 |