Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:49996725-49997099 | Common:1; Rare:83 | ||||
chr13:50081950-50082278 | Common:1; Rare:89 | ||||
chr13:50909661-50910409 | Common:3; Rare:182; Clinvar:7; Clinvar (benign):1 | ||||
chr13:51453013-51453390 | Rare:146 | ||||
chr13:51804103-51804221 | Common:2; Rare:39 | ||||
chr13:52012090-52012441 | Common:2; Rare:123; Clinvar:1 | ||||
chr13:52450064-52450182 | Rare:28 | ||||
chr13:52450568-52450723 | Common:1; Rare:46 | ||||
chr13:52455305-52455560 | Common:3; Rare:92 | ||||
chr13:52455928-52456023 | Common:1; Rare:32 | ||||
chr13:52652666-52652934 | Common:3; Rare:90 | ||||
chr13:52653070-52653186 | Common:1; Rare:37 | ||||
chr13:60163905-60164084 | Common:1; Rare:48 | ||||
chr13:67230284-67230805 | Common:2; Rare:171 | ||||
chr13:71866217-71866518 | Common:3; Rare:120 |