Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:30896458-30896635 | Common:1; Rare:42 | ||||
chr16:30923236-30923603 | Common:1; Rare:87 | ||||
chr16:31033456-31033598 | Common:1; Rare:53 | ||||
chr16:31073732-31073806 | Rare:21 | ||||
chr16:31074187-31074456 | Common:1; Rare:75 | ||||
chr16:31108268-31108465 | Rare:42 | ||||
chr16:31179829-31180179 | Common:3; Rare:145; Clinvar:2; Clinvar (benign):2 | ||||
chr16:31442772-31443059 | Common:1; Rare:47 | ||||
chr16:31459297-31459517 | Common:1; Rare:89 | ||||
chr16:31471931-31472191 | Rare:60 | ||||
chr16:31508369-31508457 | Common:1; Rare:35 | ||||
chr16:46689130-46689297 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
chr16:46973577-46973775 | Rare:87 | ||||
chr16:47461032-47461350 | Common:2; Rare:114; Clinvar (benign):2 | ||||
chr16:48244193-48244448 | Common:2; Rare:83 |