Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:29961955-29962163 | Common:1; Rare:69 | ||||
chr16:29995601-29995702 | Rare:45 | ||||
chr16:29996073-29996311 | Common:2; Rare:86 | ||||
chr16:30065560-30065916 | Rare:121 | ||||
chr16:30069660-30069981 | Common:1; Rare:113; Clinvar:3; Clinvar (benign):6 | ||||
chr16:30075889-30076069 | Common:1; Rare:63 | ||||
chr16:30113490-30113664 | Common:1; Rare:34 | ||||
chr16:30355211-30355434 | Common:1; Rare:77 | ||||
chr16:30534748-30535089 | Common:3; Rare:103 | ||||
chr16:30698449-30698639 | Common:1; Rare:74 | ||||
chr16:30762063-30762334 | Common:3; Rare:91 | ||||
chr16:30893936-30894281 | Common:5; Rare:93 | ||||
chr16:30923259-30923600 | Common:1; Rare:78 | ||||
chr16:31033273-31033581 | Common:2; Rare:99 | ||||
chr16:31074182-31074457 | Common:2; Rare:75 |