Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:36924134-36924272 | Common:1; Rare:16 | ||||
chr20:37507009-37507114 | Rare:20 | ||||
chr20:44372611-44372708 | Common:1; Rare:20 | ||||
chr20:44406813-44407038 | Rare:41 | ||||
chr20:44413456-44413750 | Common:4; Rare:57; Clinvar:3; Clinvar (benign):2 | ||||
chr20:44423748-44424254 | Common:1; Rare:111; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
chr20:45409781-45409945 | Common:1; Rare:30 | ||||
chr20:45894708-45894880 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
chr20:45898195-45898618 | Common:2; Rare:104; Clinvar:1; Clinvar (benign):1 | ||||
chr20:47318338-47318556 | Rare:48 | ||||
chr20:47331510-47331584 | Rare:10 | ||||
chr20:47357792-47357844 | Rare:11 | ||||
chr20:48985150-48985440 | Common:3; Rare:57; Clinvar (benign):1 | ||||
chr20:49221216-49221561 | Common:3; Rare:91 | ||||
chr20:49712697-49712922 | Common:5; Rare:63 |