Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:46092414-46092675 | Common:2; Rare:45 | ||||
chr21:46125462-46126126 | Common:7; Rare:337; Clinvar:48; Clinvar (benign):29; Clinvar (pathogenic):5 | ||||
chr22:19171618-19171737 | Rare:41 | ||||
chr22:19176627-19176864 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
chr22:22298061-22298208 | Common:2; Rare:56 | ||||
chr22:23717268-23717667 | Common:1; Rare:116 | ||||
chr22:26672639-26672786 | Common:2; Rare:37 | ||||
chr22:26673030-26673104 | Common:1; Rare:26 | ||||
chr22:27113278-27113454 | Common:1; Rare:33 | ||||
chr22:28799118-28799528 | Rare:76 | ||||
chr22:30182464-30182685 | Rare:26 | ||||
chr22:30196865-30197064 | Common:1; Rare:26 | ||||
chr22:30205529-30205626 | Rare:16 | ||||
chr22:30235975-30236210 | Common:1; Rare:51 | ||||
chr22:30251781-30251991 | Rare:42 |