| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:54801295-54801411 | Rare:21 | ||||
| chr1:54886528-54886843 | Common:1; Rare:108 | ||||
| chr1:54887097-54887411 | Common:2; Rare:109; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:55039255-55039630 | Common:2; Rare:85; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:56965911-56966098 | Common:1; Rare:47 | ||||
| chr1:56966110-56966183 | Rare:11 | ||||
| chr1:58546672-58546838 | Common:4; Rare:75 | ||||
| chr1:58784058-58784384 | Common:1; Rare:84 | ||||
| chr1:59296520-59296842 | Common:12; Rare:86 | ||||
| chr1:59296872-59297114 | Common:2; Rare:73 | ||||
| chr1:61076963-61077224 | Common:3; Rare:71 | ||||
| chr1:61725021-61725192 | Rare:85 | ||||
| chr1:61742345-61742538 | Rare:54 | ||||
| chr1:62597444-62598062 | Common:2; Rare:163; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr1:62688260-62688510 | Common:1; Rare:100; Clinvar:1 |