| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:9997131-9997324 | Common:2; Rare:60 | ||||
| chr1:10032670-10032980 | Common:3; Rare:86 | ||||
| chr1:10210334-10210547 | Common:4; Rare:51 | ||||
| chr1:10398765-10399108 | Common:2; Rare:127 | ||||
| chr1:10474870-10474984 | Rare:35; Clinvar:1 | ||||
| chr1:10796574-10796878 | Common:3; Rare:88 | ||||
| chr1:11099827-11099926 | Common:1; Rare:37 | ||||
| chr1:11189203-11189355 | Rare:34 | ||||
| chr1:11262490-11262817 | Common:2; Rare:101 | ||||
| chr1:11654805-11654933 | Common:2; Rare:34 | ||||
| chr1:11805900-11806276 | Common:2; Rare:102; Clinvar:1 | ||||
| chr1:11858869-11859144 | Rare:75 | ||||
| chr1:11934553-11934781 | Common:3; Rare:75; Clinvar:5; Clinvar (benign):1 | ||||
| chr1:11979892-11980473 | Common:6; Rare:157; Clinvar:1; Clinvar (benign):4 | ||||
| chr1:12229920-12230109 | Common:1; Rare:59 |