| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:9687517-9687786 | Common:3; Rare:60 | ||||
| chr1:9943291-9943488 | Common:2; Rare:47 | ||||
| chr1:10398860-10399103 | Common:2; Rare:91 | ||||
| chr1:11055875-11056087 | Rare:60 | ||||
| chr1:11099833-11099935 | Common:2; Rare:38 | ||||
| chr1:11189204-11189355 | Rare:34 | ||||
| chr1:11262515-11262850 | Common:1; Rare:95 | ||||
| chr1:11654339-11654558 | Rare:57 | ||||
| chr1:11654705-11654909 | Common:4; Rare:57 | ||||
| chr1:11805900-11806255 | Common:2; Rare:97; Clinvar:1 | ||||
| chr1:11934625-11934746 | Common:2; Rare:45; Clinvar:5 | ||||
| chr1:12618112-12618475 | Common:3; Rare:74 | ||||
| chr1:15152409-15152824 | Common:6; Rare:71 | ||||
| chr1:15153574-15153774 | Common:1; Rare:53 | ||||
| chr1:15438359-15438669 | Common:1; Rare:72; Clinvar:4; Clinvar (benign):2 |