Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16613508-16613635 | |||||
chr1:16980612-16980716 | Rare:37 | ||||
chr1:17053963-17054374 | Common:3; Rare:128; Clinvar:16; Clinvar (benign):10 | ||||
chr1:17439747-17440034 | Rare:99 | ||||
chr1:19210251-19210519 | Rare:90 | ||||
chr1:19251505-19251842 | Common:6; Rare:111 | ||||
chr1:19312033-19312352 | Common:8; Rare:154 | ||||
chr1:19485435-19485751 | Common:1; Rare:112 | ||||
chr1:19643462-19643752 | Common:2; Rare:46 | ||||
chr1:20139032-20139326 | Common:1; Rare:58 | ||||
chr1:20185916-20186128 | Common:1; Rare:70 | ||||
chr1:20508079-20508194 | Common:2; Rare:43 | ||||
chr1:20661253-20661310 | Common:1; Rare:19; Clinvar:1; Clinvar (benign):1 | ||||
chr1:20787196-20787416 | Rare:107 | ||||
chr1:21176836-21177092 | Rare:73 |