Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:82900463-82900759 | Rare:85 | ||||
chr4:82900906-82901060 | Rare:63 | ||||
chr4:83455800-83456065 | Common:2; Rare:101 | ||||
chr4:86934892-86935054 | Common:2; Rare:72 | ||||
chr4:88007503-88007691 | Common:2; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
chr4:88523696-88523875 | Common:2; Rare:58 | ||||
chr4:99088693-99088922 | Common:7; Rare:109 | ||||
chr4:99950271-99950528 | Rare:53 | ||||
chr4:101347449-101347816 | Common:5; Rare:110 | ||||
chr4:102826837-102827186 | Common:4; Rare:121 | ||||
chr4:102828007-102828100 | Rare:32 | ||||
chr4:102868830-102869012 | Common:1; Rare:59 | ||||
chr4:103019638-103019683 | Rare:9 | ||||
chr4:105708646-105708801 | Rare:45 | ||||
chr4:106316191-106316621 | Common:5; Rare:138 |