Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:46364362-46364538 | Rare:67 | ||||
chr20:46406571-46406783 | Common:2; Rare:52 | ||||
chr20:46513536-46513704 | Common:3; Rare:64 | ||||
chr20:46689148-46689213 | Rare:16; Clinvar (pathogenic):1 | ||||
chr20:47318703-47319027 | Common:1; Rare:102 | ||||
chr20:47356664-47356887 | Rare:51 | ||||
chr20:47501551-47502132 | Common:2; Rare:177 | ||||
chr20:49219281-49219502 | Rare:106 | ||||
chr20:49278036-49278278 | Rare:67 | ||||
chr20:49568058-49568376 | Common:10; Rare:78 | ||||
chr20:49915487-49915553 | Rare:24 | ||||
chr20:50113112-50113428 | Common:6; Rare:104 | ||||
chr20:50153647-50153887 | Common:2; Rare:96 | ||||
chr20:50958467-50958874 | Common:1; Rare:156; Clinvar:2; Clinvar (benign):4 | ||||
chr20:53593797-53593894 | Common:1; Rare:35 |