Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:89080581-89080838 | Common:1; Rare:108 | ||||
chr6:89081048-89081416 | Common:2; Rare:139 | ||||
chr6:89145983-89146132 | Rare:48 | ||||
chr6:89638411-89638549 | Common:1; Rare:31 | ||||
chr6:89638712-89638845 | Common:3; Rare:48 | ||||
chr6:89829595-89829942 | Rare:89 | ||||
chr6:93419552-93419796 | Common:1; Rare:65 | ||||
chr6:95577404-95577584 | Common:5; Rare:53 | ||||
chr6:96521665-96521876 | Common:8; Rare:101 | ||||
chr6:96897771-96898083 | Common:4; Rare:119; Clinvar:4; Clinvar (benign):1 | ||||
chr6:99424668-99424963 | Rare:81 | ||||
chr6:99425214-99425425 | Common:1; Rare:64 | ||||
chr6:99425678-99425717 | Rare:13 | ||||
chr6:100881167-100881482 | Common:6; Rare:115 | ||||
chr6:105137031-105137276 | Common:1; Rare:87 |