Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:9555730-9555992 | Common:2; Rare:86 | ||||
chr2:17540445-17540714 | Common:1; Rare:64 | ||||
chr2:17753738-17753891 | Common:1; Rare:54 | ||||
chr2:19990079-19990220 | Rare:36 | ||||
chr2:23940379-23940506 | Common:3; Rare:44 | ||||
chr2:24076280-24076594 | Rare:80 | ||||
chr2:24123255-24123489 | Common:1; Rare:59 | ||||
chr2:26244600-26244965 | Common:2; Rare:131; Clinvar:5; Clinvar (benign):7 | ||||
chr2:26764201-26764325 | Common:1; Rare:48 | ||||
chr2:27323043-27323150 | Rare:27; Clinvar (benign):1 | ||||
chr2:27356754-27357067 | Rare:89 | ||||
chr2:27370319-27370641 | Common:1; Rare:128 | ||||
chr2:27628872-27629058 | Common:1; Rare:79 | ||||
chr2:27663604-27663911 | Rare:109 | ||||
chr2:28751698-28752081 | Common:2; Rare:162 |