Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43058748-43058798 | Rare:15 | ||||
chr1:43068164-43068274 | Common:3; Rare:25 | ||||
chr1:43068485-43068518 | Rare:5 | ||||
chr1:43120494-43120563 | Rare:17 | ||||
chr1:43206694-43207213 | Common:1; Rare:126 | ||||
chr1:43207603-43207845 | Common:1; Rare:41 | ||||
chr1:43274395-43274480 | Rare:10 | ||||
chr1:43274509-43274680 | Rare:21 | ||||
chr1:43330331-43330490 | Common:1; Rare:21 | ||||
chr1:43348898-43349136 | Common:1; Rare:84; Clinvar:3; Clinvar (benign):1 | ||||
chr1:43349450-43349685 | Rare:46 | ||||
chr1:43454580-43454873 | Common:1; Rare:62 | ||||
chr1:43531623-43531641 | Rare:3 | ||||
chr1:43763421-43763760 | Rare:58 | ||||
chr1:43853267-43853302 | Rare:8 |