Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44631902-44632160 | Common:3; Rare:93 | ||||
chr1:44674425-44674731 | Common:3; Rare:76 | ||||
chr1:44775462-44775607 | Rare:55 | ||||
chr1:44775841-44776138 | Common:2; Rare:107 | ||||
chr1:45339987-45340046 | Rare:18 | ||||
chr1:45340118-45340193 | Rare:33 | ||||
chr1:45340385-45340505 | Common:1; Rare:32; Clinvar:1 | ||||
chr1:45500040-45500356 | Common:1; Rare:77; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521865-45522074 | Common:1; Rare:83 | ||||
chr1:45550730-45551098 | Common:3; Rare:89 | ||||
chr1:45583931-45584085 | Rare:60 | ||||
chr1:45687059-45687274 | Common:1; Rare:64 | ||||
chr1:45688042-45688228 | Common:1; Rare:53 | ||||
chr1:45750622-45750814 | Rare:70 | ||||
chr1:45803492-45803614 | Common:1; Rare:42 |