Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:31074187-31074438 | Common:1; Rare:68 | ||||
chr16:31508374-31508484 | Common:2; Rare:43 | ||||
chr16:46689140-46689405 | Common:1; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
chr16:46973603-46973781 | Rare:79 | ||||
chr16:47461046-47461350 | Common:2; Rare:105; Clinvar (benign):2 | ||||
chr16:53703828-53704162 | Rare:95; Clinvar:3 | ||||
chr16:56451289-56451605 | Common:1; Rare:103 | ||||
chr16:56729950-56730198 | Common:1; Rare:60 | ||||
chr16:57185793-57186335 | Common:3; Rare:145 | ||||
chr16:57447360-57447499 | Common:2; Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
chr16:58001318-58001440 | Rare:33 | ||||
chr16:58129311-58129567 | Common:2; Rare:80 | ||||
chr16:58734236-58734391 | Common:4; Rare:50 | ||||
chr16:66552469-66552639 | Rare:74 | ||||
chr16:66934341-66934474 | Common:1; Rare:57 |