Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:31472109-31472188 | Rare:21 | ||||
chr16:31508374-31508464 | Common:1; Rare:33 | ||||
chr16:46689134-46689286 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
chr16:46973544-46973796 | Rare:107 | ||||
chr16:47461032-47461378 | Common:2; Rare:135; Clinvar (benign):2 | ||||
chr16:48244257-48244532 | Common:2; Rare:83 | ||||
chr16:48385302-48385543 | Common:3; Rare:97 | ||||
chr16:50245918-50246174 | Common:2; Rare:59 | ||||
chr16:50742727-50742803 | Rare:11 | ||||
chr16:53434677-53434730 | Common:1; Rare:18 | ||||
chr16:53703821-53704187 | Rare:107; Clinvar:4; Clinvar (benign):1 | ||||
chr16:55478727-55478891 | Common:1; Rare:30 | ||||
chr16:55479037-55479214 | Rare:42 | ||||
chr16:55479572-55479618 | Rare:14; Clinvar:1 | ||||
chr16:55480733-55480964 | Common:1; Rare:36 |