Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174999621-175000145 | Common:3; Rare:166 | ||||
chr1:178725114-178725335 | Common:10; Rare:81 | ||||
chr1:179882223-179882306 | Rare:16 | ||||
chr1:179882488-179882878 | Rare:190; Clinvar:8; Clinvar (benign):2 | ||||
chr1:180502352-180502650 | Common:1; Rare:103 | ||||
chr1:181088519-181088704 | Rare:62 | ||||
chr1:182839302-182839418 | Rare:57 | ||||
chr1:183635640-183636110 | Common:5; Rare:131 | ||||
chr1:184051629-184051753 | Common:2; Rare:47 | ||||
chr1:184754812-184755107 | Common:1; Rare:67 | ||||
chr1:185045241-185045576 | Common:1; Rare:116 | ||||
chr1:185156923-185157297 | Common:1; Rare:101 | ||||
chr1:185157348-185157527 | Common:1; Rare:55 | ||||
chr1:185317196-185317468 | Common:1; Rare:81 | ||||
chr1:186375132-186375523 | Rare:103 |