Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:29996072-29996296 | Common:2; Rare:79 | ||||
chr16:30065511-30065857 | Rare:116 | ||||
chr16:30075878-30076059 | Common:1; Rare:60 | ||||
chr16:30355219-30355481 | Common:2; Rare:87 | ||||
chr16:30762110-30762331 | Common:3; Rare:83 | ||||
chr16:30893960-30894262 | Common:5; Rare:80 | ||||
chr16:31074217-31074432 | Common:1; Rare:58 | ||||
chr16:31108373-31108458 | Rare:29 | ||||
chr16:31471931-31472191 | Rare:60 | ||||
chr16:31508389-31508504 | Common:4; Rare:47 | ||||
chr16:46689140-46689384 | Common:1; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
chr16:46689543-46689714 | Common:2; Rare:77; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr16:46973583-46973757 | Rare:78 | ||||
chr16:47461032-47461348 | Common:2; Rare:114; Clinvar (benign):2 | ||||
chr16:53054803-53055029 | Common:2; Rare:56 |