Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:31459296-31459517 | Common:1; Rare:90 | ||||
chr16:31472080-31472191 | Rare:31 | ||||
chr16:31508374-31508478 | Common:1; Rare:41 | ||||
chr16:46689130-46689313 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
chr16:46973627-46973768 | Rare:66 | ||||
chr16:47461002-47461365 | Common:2; Rare:143; Clinvar (benign):2 | ||||
chr16:48385302-48385537 | Common:3; Rare:95 | ||||
chr16:50693498-50693626 | Rare:51 | ||||
chr16:53503177-53503494 | Common:8; Rare:96 | ||||
chr16:53703828-53704179 | Rare:99; Clinvar:3 | ||||
chr16:54286625-54287011 | Common:2; Rare:104 | ||||
chr16:55478974-55479207 | Common:1; Rare:55 | ||||
chr16:56336428-56336523 | Common:1; Rare:21 | ||||
chr16:56451306-56451605 | Common:1; Rare:98 | ||||
chr16:56608307-56608680 | Common:3; Rare:105 |