Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:28846271-28846636 | Common:2; Rare:122; Clinvar:5; Clinvar (benign):5 | ||||
chr16:28974647-28974786 | Common:1; Rare:59 | ||||
chr16:29816000-29816200 | Common:1; Rare:57 | ||||
chr16:29961989-29962141 | Common:1; Rare:45 | ||||
chr16:29995610-29995736 | Rare:56 | ||||
chr16:29996073-29996296 | Common:2; Rare:78 | ||||
chr16:30064345-30064479 | Common:1; Rare:24; Clinvar (benign):1 | ||||
chr16:30075894-30076045 | Rare:50 | ||||
chr16:30123099-30123371 | Common:6; Rare:75 | ||||
chr16:30355210-30355434 | Common:1; Rare:78 | ||||
chr16:30534838-30535070 | Common:2; Rare:74 | ||||
chr16:30558405-30558669 | Common:2; Rare:70 | ||||
chr16:30698469-30698590 | Common:1; Rare:52 | ||||
chr16:30762060-30762325 | Common:3; Rare:91 | ||||
chr16:30893948-30894268 | Common:5; Rare:87 |