Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:23678689-23678927 | Common:4; Rare:71 | ||||
chr16:25111452-25111758 | Common:2; Rare:71 | ||||
chr16:27268719-27268872 | Common:1; Rare:52 | ||||
chr16:27549886-27550167 | Common:2; Rare:104 | ||||
chr16:28846271-28846648 | Common:2; Rare:127; Clinvar:5; Clinvar (benign):5 | ||||
chr16:29961942-29962126 | Common:1; Rare:54 | ||||
chr16:29995608-29995706 | Rare:44 | ||||
chr16:29996076-29996296 | Common:2; Rare:77 | ||||
chr16:30065434-30065855 | Rare:135 | ||||
chr16:30075887-30076040 | Rare:51 | ||||
chr16:30355264-30355322 | Rare:17 | ||||
chr16:30748116-30748441 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
chr16:30762060-30762334 | Common:3; Rare:93 | ||||
chr16:31459359-31459408 | Rare:23 | ||||
chr16:31508389-31508478 | Common:1; Rare:34 |