Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43368003-43368180 | Rare:46 | ||||
chr1:43389757-43389922 | Common:3; Rare:71 | ||||
chr1:44030863-44031080 | Rare:52 | ||||
chr1:44775455-44775599 | Rare:56 | ||||
chr1:44777621-44778067 | Common:2; Rare:112 | ||||
chr1:45012065-45012258 | Common:1; Rare:71; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45500016-45500335 | Common:2; Rare:73; Clinvar:4; Clinvar (pathogenic):2 | ||||
chr1:45688091-45688222 | Common:1; Rare:39 | ||||
chr1:46198426-46198519 | Common:1; Rare:35 | ||||
chr1:46303301-46303778 | Common:2; Rare:133 | ||||
chr1:46340672-46340801 | Common:2; Rare:33 | ||||
chr1:47314110-47314410 | Common:3; Rare:60; Clinvar:1 | ||||
chr1:52055186-52055265 | Rare:20 | ||||
chr1:52056163-52056338 | Rare:55 | ||||
chr1:52404340-52404626 | Common:1; Rare:75 |