Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:31108354-31108458 | Rare:30 | ||||
chr16:31135647-31135838 | Rare:46 | ||||
chr16:31202641-31202955 | Common:2; Rare:109 | ||||
chr16:31459296-31459510 | Common:1; Rare:88 | ||||
chr16:31471931-31472183 | Rare:56 | ||||
chr16:31508374-31508484 | Common:2; Rare:43 | ||||
chr16:46689131-46689286 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
chr16:46973537-46973775 | Rare:97 | ||||
chr16:47461041-47461350 | Common:2; Rare:108; Clinvar (benign):2 | ||||
chr16:48244227-48244598 | Common:2; Rare:105 | ||||
chr16:50693505-50693626 | Rare:49 | ||||
chr16:53703821-53704179 | Rare:101; Clinvar:3; Clinvar (benign):1 | ||||
chr16:54286397-54286431 | Rare:3 | ||||
chr16:54286670-54287030 | Common:2; Rare:107 | ||||
chr16:56451263-56451592 | Common:1; Rare:98 |