Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19210071-19210533 | Common:1; Rare:150 | ||||
chr1:19251494-19251863 | Common:6; Rare:124 | ||||
chr1:19311982-19312356 | Common:8; Rare:169 | ||||
chr1:19485435-19485765 | Common:1; Rare:124 | ||||
chr1:19596676-19597080 | Common:3; Rare:139 | ||||
chr1:19799716-19799980 | Common:4; Rare:84 | ||||
chr1:19979547-19979973 | Common:5; Rare:76 | ||||
chr1:20185924-20186128 | Common:1; Rare:68 | ||||
chr1:20486228-20486379 | Rare:36 | ||||
chr1:20508020-20508194 | Common:2; Rare:60 | ||||
chr1:20661345-20661663 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786555-20786870 | Rare:112 | ||||
chr1:20787197-20787416 | Rare:107 | ||||
chr1:21176852-21177108 | Rare:72 | ||||
chr1:21345467-21345655 | Common:2; Rare:73 |