| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42846401-42846638 | Common:1; Rare:65 | ||||
| chr1:42958785-42959095 | Common:4; Rare:83; Clinvar:6; Clinvar (benign):4 | ||||
| chr1:43172218-43172352 | Common:1; Rare:66 | ||||
| chr1:43367946-43368212 | Rare:68 | ||||
| chr1:43389747-43389964 | Common:4; Rare:98 | ||||
| chr1:43649833-43650187 | Rare:84 | ||||
| chr1:43707355-43707576 | Common:2; Rare:63 | ||||
| chr1:43979874-43979962 | Rare:24 | ||||
| chr1:44674421-44674731 | Common:3; Rare:79 | ||||
| chr1:44811216-44811332 | Common:1; Rare:31 | ||||
| chr1:45012044-45012283 | Common:1; Rare:85; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:45339996-45340243 | Rare:87; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr1:45499960-45500358 | Common:2; Rare:92; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr1:45521843-45522064 | Common:1; Rare:90 | ||||
| chr1:45687027-45687350 | Common:2; Rare:84 |