| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42658295-42658480 | Common:2; Rare:56 | ||||
| chr1:42767023-42767314 | Common:5; Rare:91 | ||||
| chr1:42846387-42846636 | Common:1; Rare:73 | ||||
| chr1:42958821-42959042 | Common:3; Rare:61; Clinvar:5; Clinvar (benign):4 | ||||
| chr1:43172198-43172335 | Common:1; Rare:60 | ||||
| chr1:43358662-43359054 | Common:7; Rare:128 | ||||
| chr1:43367937-43368216 | Rare:69 | ||||
| chr1:43389765-43389956 | Common:4; Rare:83 | ||||
| chr1:44213379-44213498 | Common:1; Rare:25 | ||||
| chr1:44674425-44674744 | Common:3; Rare:80 | ||||
| chr1:44739674-44739925 | Common:1; Rare:98 | ||||
| chr1:44775447-44775603 | Rare:58 | ||||
| chr1:45011884-45012262 | Common:5; Rare:100; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:45339964-45340243 | Rare:100; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr1:45500059-45500361 | Common:1; Rare:73; Clinvar:4; Clinvar (pathogenic):3 |