Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:150583528-150583694 | Rare:33 | ||||
chr4:151100791-151101161 | Rare:76 | ||||
chr4:153023189-153023377 | Common:3; Rare:44 | ||||
chr4:153024116-153024261 | Common:3; Rare:26 | ||||
chr4:154560284-154560522 | Common:3; Rare:43 | ||||
chr4:154571993-154572588 | Common:5; Rare:116; Clinvar:7; Clinvar (benign):4 | ||||
chr4:154588698-154589010 | Rare:88; Clinvar:3 | ||||
chr4:154589428-154589704 | Rare:77; Clinvar:3; Clinvar (pathogenic):2 | ||||
chr4:154606588-154607069 | Rare:112; Clinvar:10 | ||||
chr4:169626329-169626352 | Rare:2 | ||||
chr4:176320505-176320640 | Rare:43 | ||||
chr4:182881000-182881153 | Common:2; Rare:31 | ||||
chr4:184348807-184349051 | Rare:49 | ||||
chr4:184537548-184537743 | Common:3; Rare:49 | ||||
chr4:184813387-184813693 | Common:2; Rare:65 |