Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:185425901-185426252 | Common:2; Rare:99 | ||||
chr4:189940588-189940904 | Common:8; Rare:100 | ||||
chr5:218134-218361 | Common:3; Rare:90; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr5:443130-443263 | Common:7; Rare:52 | ||||
chr5:892732-892941 | Common:2; Rare:81 | ||||
chr5:1799795-1799986 | Common:4; Rare:91 | ||||
chr5:1801356-1801420 | Common:1; Rare:23; Clinvar (benign):1 | ||||
chr5:7869004-7869194 | Common:2; Rare:92; Clinvar (benign):1 | ||||
chr5:16465768-16465913 | Rare:30 | ||||
chr5:31532070-31532319 | Common:1; Rare:66 | ||||
chr5:33440706-33441030 | Common:3; Rare:89 | ||||
chr5:34915483-34915741 | Common:1; Rare:62 | ||||
chr5:36151885-36152120 | Rare:66 | ||||
chr5:40755899-40756093 | Rare:53 | ||||
chr5:40798151-40798345 | Rare:76 |