Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:182917305-182917575 | Common:4; Rare:84 | ||||
chr4:183659122-183659343 | Common:1; Rare:69 | ||||
chr4:184474504-184474810 | Rare:68 | ||||
chr4:184649406-184649756 | Common:4; Rare:117 | ||||
chr4:185425866-185426240 | Common:3; Rare:115 | ||||
chr4:185811723-185811871 | Common:1; Rare:31 | ||||
chr4:189940649-189940941 | Common:8; Rare:103 | ||||
chr5:218140-218362 | Common:3; Rare:90; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr5:1799795-1799988 | Common:4; Rare:92 | ||||
chr5:1801300-1801436 | Common:4; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
chr5:6378492-6378678 | Rare:78 | ||||
chr5:7869000-7869201 | Common:2; Rare:101; Clinvar (benign):1 | ||||
chr5:10353573-10353908 | Common:3; Rare:129 | ||||
chr5:14581643-14581873 | Rare:101 | ||||
chr5:16465529-16465944 | Common:1; Rare:120 |