Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174022306-174022469 | Rare:42 | ||||
chr1:174159274-174159596 | Common:4; Rare:113 | ||||
chr1:174964649-174964845 | Rare:33 | ||||
chr1:174999314-174999492 | Common:1; Rare:47 | ||||
chr1:174999807-175000164 | Common:3; Rare:126 | ||||
chr1:176207242-176207344 | Common:1; Rare:50 | ||||
chr1:177969902-177970270 | Common:1; Rare:78 | ||||
chr1:177970273-177970297 | Rare:6 | ||||
chr1:178094387-178094486 | Rare:46 | ||||
chr1:178724948-178725344 | Common:11; Rare:128 | ||||
chr1:178871027-178871192 | Rare:29 | ||||
chr1:179081889-179082106 | Common:1; Rare:67 | ||||
chr1:179229670-179229865 | Common:4; Rare:31 | ||||
chr1:179881921-179882341 | Common:4; Rare:101 | ||||
chr1:179882488-179882907 | Rare:210; Clinvar:9; Clinvar (benign):2 |