Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:171741918-171742122 | Common:1; Rare:65 | ||||
chr1:173476994-173477484 | Common:5; Rare:163 | ||||
chr1:173714874-173715055 | Common:1; Rare:43 | ||||
chr1:173824390-173824702 | Rare:57; Clinvar:1 | ||||
chr1:173867970-173868161 | Rare:73 | ||||
chr1:174159173-174159560 | Common:6; Rare:134 | ||||
chr1:174999773-175000145 | Common:3; Rare:121 | ||||
chr1:178341332-178341539 | Common:1; Rare:41 | ||||
chr1:178725036-178725335 | Common:10; Rare:105 | ||||
chr1:179882069-179882306 | Common:1; Rare:55 | ||||
chr1:179882388-179882837 | Rare:190; Clinvar:7; Clinvar (benign):2 | ||||
chr1:181088494-181088711 | Rare:71 | ||||
chr1:183635666-183636056 | Common:2; Rare:107 | ||||
chr1:185156699-185156754 | Rare:30 | ||||
chr1:185156927-185157303 | Common:1; Rare:103 |