Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:182143814-182143963 | Common:2; Rare:32 | ||||
chr4:183504391-183504628 | Rare:87 | ||||
chr4:183659162-183659323 | Rare:48 | ||||
chr4:184474509-184474696 | Rare:41 | ||||
chr4:184649436-184649775 | Common:4; Rare:110 | ||||
chr4:185396431-185397249 | Rare:295 | ||||
chr4:185425951-185426255 | Common:2; Rare:79 | ||||
chr4:185471054-185471422 | Common:10; Rare:49 | ||||
chr4:186191742-186191934 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
chr4:189940620-189940991 | Common:11; Rare:133 | ||||
chr5:218114-218349 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):2 | ||||
chr5:443068-443288 | Common:10; Rare:103 | ||||
chr5:612197-612357 | Rare:64 | ||||
chr5:644077-644319 | Rare:78 | ||||
chr5:892529-892981 | Common:5; Rare:140 |