Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:185734950-185735105 | Common:2; Rare:23 | ||||
chr5:1594456-1594753 | Common:3; Rare:103 | ||||
chr5:8457537-8457741 | Common:2; Rare:74 | ||||
chr5:9363014-9363277 | Common:2; Rare:43 | ||||
chr5:34864279-34864464 | Rare:34 | ||||
chr5:43066972-43067041 | Rare:16 | ||||
chr5:55425953-55426161 | Common:2; Rare:80 | ||||
chr5:55944379-55944618 | Rare:51 | ||||
chr5:80650902-80651185 | Common:2; Rare:54 | ||||
chr5:112160826-112160920 | Common:2; Rare:51 | ||||
chr5:113807843-113808035 | Common:1; Rare:45 | ||||
chr5:128083058-128083159 | Common:2; Rare:28 | ||||
chr5:128345572-128345606 | Rare:12; Clinvar:1; Clinvar (benign):2 | ||||
chr5:129152319-129152475 | Common:3; Rare:28 | ||||
chr5:132487998-132488191 | Common:1; Rare:39 |