Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:151452010-151452552 | Common:5; Rare:190; Clinvar (benign):3 | ||||
chr6:152302124-152302240 | Rare:32 | ||||
chr6:152983030-152983281 | Common:2; Rare:76 | ||||
chr6:152983610-152983768 | Common:3; Rare:59 | ||||
chr6:153002622-153002838 | Common:3; Rare:81 | ||||
chr6:153131118-153131491 | Rare:142 | ||||
chr6:154733165-154733499 | Rare:145 | ||||
chr6:155216678-155216854 | Common:1; Rare:30 | ||||
chr6:155216858-155217028 | Rare:28 | ||||
chr6:155314426-155314613 | Common:4; Rare:67 | ||||
chr6:157323501-157323602 | Common:2; Rare:35 | ||||
chr6:158168160-158168402 | Common:3; Rare:91; Clinvar:1 | ||||
chr6:158312682-158312874 | Common:5; Rare:46 | ||||
chr6:158536465-158536728 | Common:1; Rare:120 | ||||
chr6:158644670-158644833 | Common:3; Rare:83 |