| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:9943300-9943488 | Common:2; Rare:42 | ||||
| chr1:10032795-10032961 | Rare:50 | ||||
| chr1:10210334-10210555 | Common:4; Rare:55 | ||||
| chr1:10398819-10399103 | Common:2; Rare:109 | ||||
| chr1:10449829-10450196 | Common:1; Rare:95 | ||||
| chr1:10474889-10475032 | Rare:60; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:11099779-11099922 | Common:1; Rare:63 | ||||
| chr1:11262493-11262839 | Common:2; Rare:101 | ||||
| chr1:11478852-11479169 | Common:4; Rare:93 | ||||
| chr1:11654773-11654925 | Common:2; Rare:47 | ||||
| chr1:11691477-11691786 | Common:4; Rare:72 | ||||
| chr1:11805970-11806268 | Common:2; Rare:76 | ||||
| chr1:11980080-11980465 | Common:6; Rare:120; Clinvar:1; Clinvar (benign):4 | ||||
| chr1:12019278-12019501 | Common:5; Rare:73 | ||||
| chr1:13749224-13749451 | Common:2; Rare:77 |