Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26306614-26306860 | Common:13; Rare:75 | ||||
chr1:26410666-26410894 | Rare:67 | ||||
chr1:26432090-26432390 | Common:5; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472304-26472528 | Common:4; Rare:74 | ||||
chr1:26787865-26787974 | Common:1; Rare:36; Clinvar (benign):1 | ||||
chr1:26890229-26890359 | Common:1; Rare:50 | ||||
chr1:26900435-26900547 | Rare:37 | ||||
chr1:26921549-26921804 | Common:3; Rare:77 | ||||
chr1:27725762-27725984 | Common:2; Rare:56 | ||||
chr1:27772923-27773269 | Common:1; Rare:107 | ||||
chr1:28088551-28088796 | Common:3; Rare:82 | ||||
chr1:28328910-28329073 | Common:1; Rare:49 | ||||
chr1:28369636-28369802 | Common:1; Rare:69 | ||||
chr1:28505807-28506050 | Common:2; Rare:92 | ||||
chr1:28552867-28553108 | Common:2; Rare:91 |