Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:85613046-85613338 | Common:1; Rare:110 | ||||
chr16:85799532-85799748 | Common:2; Rare:63 | ||||
chr16:85804770-85805064 | Common:3; Rare:85 | ||||
chr16:86555180-86555288 | Rare:54 | ||||
chr16:87317348-87317516 | Common:5; Rare:67 | ||||
chr16:87765911-87766017 | Rare:44 | ||||
chr16:88570174-88570498 | Common:1; Rare:123 | ||||
chr16:88663084-88663362 | Common:7; Rare:113 | ||||
chr16:88706283-88706542 | Common:4; Rare:123 | ||||
chr16:88856941-88857156 | Common:4; Rare:95; Clinvar (benign):2 | ||||
chr16:89217619-89217738 | Common:1; Rare:56 | ||||
chr16:89508285-89508420 | Rare:75; Clinvar (pathogenic):1 | ||||
chr16:89560564-89560717 | Rare:63 | ||||
chr16:89657632-89658058 | Common:3; Rare:223 | ||||
chr16:89686590-89686704 | Common:6; Rare:55 |