| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161098304-161098444 | Common:1; Rare:31 | ||||
| chr1:161117977-161118141 | Rare:87 | ||||
| chr1:161132356-161132862 | Common:2; Rare:153 | ||||
| chr1:161159392-161159536 | Common:1; Rare:43 | ||||
| chr1:161166228-161166512 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:161197168-161197419 | Common:3; Rare:40 | ||||
| chr1:161199046-161199304 | Rare:42 | ||||
| chr1:161215090-161215357 | Common:2; Rare:81 | ||||
| chr1:161223611-161223861 | Rare:45; Clinvar:1 | ||||
| chr1:161309951-161310225 | Common:1; Rare:41; Clinvar:1 | ||||
| chr1:161314262-161314425 | Common:3; Rare:65; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr1:161524375-161524546 | Common:3; Rare:55 | ||||
| chr1:161549794-161549898 | Rare:36 | ||||
| chr1:161550613-161550796 | Common:2; Rare:33 | ||||
| chr1:161631092-161631212 | Common:2; Rare:52 |