Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150067690-150067866 | Rare:55 | ||||
chr1:150293825-150293909 | Rare:30 | ||||
chr1:150364596-150364717 | Rare:41 | ||||
chr1:150487265-150487446 | Common:3; Rare:43; Clinvar (benign):3 | ||||
chr1:150578516-150578699 | Common:1; Rare:54 | ||||
chr1:150579553-150579846 | Common:10; Rare:106 | ||||
chr1:150629088-150629398 | Common:1; Rare:99 | ||||
chr1:150629461-150629858 | Common:1; Rare:91 | ||||
chr1:150697025-150697263 | Common:1; Rare:47 | ||||
chr1:150876563-150876869 | Common:5; Rare:115 | ||||
chr1:150926303-150926454 | Rare:44 | ||||
chr1:150982190-150982343 | Common:2; Rare:25 | ||||
chr1:151008357-151008539 | Common:1; Rare:60 | ||||
chr1:151156478-151156684 | Rare:36 | ||||
chr1:151165840-151166171 | Common:3; Rare:93 |