Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:29996141-29996289 | Common:1; Rare:55 | ||||
chr16:30065434-30065841 | Rare:132 | ||||
chr16:30075883-30076045 | Rare:53 | ||||
chr16:30534773-30535068 | Common:2; Rare:89 | ||||
chr16:30762213-30762327 | Common:3; Rare:61 | ||||
chr16:30923256-30923561 | Common:1; Rare:75 | ||||
chr16:46973606-46973775 | Rare:79 | ||||
chr16:47461041-47461350 | Common:2; Rare:108; Clinvar (benign):2 | ||||
chr16:53703821-53704195 | Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
chr16:56451306-56451573 | Common:1; Rare:75 | ||||
chr16:56519975-56520125 | Common:4; Rare:60; Clinvar:6; Clinvar (benign):5 | ||||
chr16:56608352-56608756 | Common:4; Rare:118 | ||||
chr16:56729975-56730192 | Common:1; Rare:50 | ||||
chr16:56931909-56932147 | Common:2; Rare:112 | ||||
chr16:57185990-57186335 | Common:1; Rare:99 |