Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:148458673-148458975 | Common:2; Rare:80 | ||||
chr1:149390414-149390634 | Rare:30 | ||||
chr1:149886671-149887024 | Common:1; Rare:124 | ||||
chr1:149887952-149888215 | Rare:57 | ||||
chr1:149927766-149927891 | Common:1; Rare:45; Clinvar (benign):4 | ||||
chr1:150067651-150067860 | Rare:64 | ||||
chr1:150321413-150321592 | Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150363928-150364201 | Common:4; Rare:96 | ||||
chr1:150487273-150487445 | Common:3; Rare:39; Clinvar (benign):3 | ||||
chr1:150578469-150579015 | Common:5; Rare:181 | ||||
chr1:150579582-150579864 | Common:10; Rare:92 | ||||
chr1:150629107-150629314 | Rare:58 | ||||
chr1:150629450-150629825 | Rare:83 | ||||
chr1:150697014-150697461 | Common:1; Rare:92 | ||||
chr1:150876560-150876869 | Common:5; Rare:115 |