Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:5950414-5950695 | Common:8; Rare:86 | ||||
chr20:13784892-13785053 | Common:2; Rare:65; Clinvar (benign):2 | ||||
chr20:17569949-17570193 | Common:3; Rare:106 | ||||
chr20:17968444-17968605 | Common:4; Rare:70 | ||||
chr20:17968795-17969090 | Common:2; Rare:111 | ||||
chr20:21303096-21303385 | Rare:100 | ||||
chr20:24992698-24992826 | Common:3; Rare:59 | ||||
chr20:31722851-31722956 | Rare:26 | ||||
chr20:32207703-32207934 | Common:3; Rare:89 | ||||
chr20:34677086-34677325 | Rare:60 | ||||
chr20:35699336-35699460 | Rare:38 | ||||
chr20:35742175-35742584 | Common:4; Rare:124 | ||||
chr20:37289545-37289669 | Common:1; Rare:36 | ||||
chr20:37527863-37528191 | Common:5; Rare:116 | ||||
chr20:38033415-38033775 | Common:2; Rare:105 |