Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:92833393-92833639 | Common:1; Rare:62; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:92835680-92835773 | Rare:20 | ||||
chr1:93332513-93333007 | Common:3; Rare:78 | ||||
chr1:93339392-93339490 | Common:2; Rare:16 | ||||
chr1:93347243-93347478 | Rare:45 | ||||
chr1:93498185-93498258 | Rare:8 | ||||
chr1:93571761-93572080 | Common:1; Rare:87 | ||||
chr1:93680417-93680567 | Common:1; Rare:21 | ||||
chr1:94247589-94247870 | Common:3; Rare:84 | ||||
chr1:94863983-94864292 | Rare:47 | ||||
chr1:94926418-94926529 | Rare:21 | ||||
chr1:96777900-96778151 | Common:2; Rare:58 | ||||
chr1:96800617-96800775 | Rare:29 | ||||
chr1:97081517-97081668 | Rare:22 | ||||
chr1:97081810-97081871 | Rare:10 |