Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:30997290-30997421 | Common:1; Rare:31 | ||||
chr16:31033343-31033576 | Common:1; Rare:80 | ||||
chr16:31074187-31074451 | Common:1; Rare:73 | ||||
chr16:31471931-31472186 | Rare:58 | ||||
chr16:31508389-31508448 | Rare:23 | ||||
chr16:46689134-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
chr16:46973603-46973775 | Rare:79 | ||||
chr16:47461032-47461343 | Common:2; Rare:110; Clinvar (benign):1 | ||||
chr16:48244253-48244360 | Common:1; Rare:34 | ||||
chr16:53098912-53099184 | Rare:59 | ||||
chr16:53703814-53704192 | Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
chr16:56451296-56451605 | Common:1; Rare:101 | ||||
chr16:56608318-56608737 | Common:4; Rare:122 | ||||
chr16:56632450-56632664 | Common:2; Rare:64 | ||||
chr16:56682244-56682486 | Common:3; Rare:72 |