Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:169660036-169660254 | Common:1; Rare:41 | ||||
chr4:174283599-174283938 | Common:1; Rare:66 | ||||
chr4:177442384-177442514 | Rare:76; Clinvar:2 | ||||
chr4:182917295-182917551 | Common:4; Rare:84 | ||||
chr4:183659122-183659396 | Common:1; Rare:90 | ||||
chr4:184474504-184474816 | Rare:69 | ||||
chr4:184649406-184649752 | Common:4; Rare:113 | ||||
chr4:185396596-185396843 | Rare:81 | ||||
chr4:185425880-185426272 | Common:4; Rare:116 | ||||
chr5:218114-218362 | Common:3; Rare:101; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr5:1799790-1799986 | Common:5; Rare:92 | ||||
chr5:1801375-1801447 | Common:1; Rare:41; Clinvar:3; Clinvar (benign):1 | ||||
chr5:7869000-7869204 | Common:2; Rare:103; Clinvar (benign):1 | ||||
chr5:9546017-9546356 | Common:9; Rare:87 | ||||
chr5:9546367-9546517 | Common:3; Rare:27 |