Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:15741747-15742074 | Common:1; Rare:91; Clinvar:3; Clinvar (benign):3 | ||||
chr16:15856946-15857151 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2 | ||||
chr16:18926387-18926614 | Common:2; Rare:96 | ||||
chr16:19067830-19067920 | Common:1; Rare:19 | ||||
chr16:19113663-19113969 | Common:1; Rare:55 | ||||
chr16:19691190-19691298 | Common:1; Rare:19 | ||||
chr16:19884824-19884994 | Common:2; Rare:58 | ||||
chr16:20676154-20676263 | Common:2; Rare:19 | ||||
chr16:20741735-20741915 | Common:1; Rare:84 | ||||
chr16:20763942-20764050 | Common:1; Rare:20 | ||||
chr16:20806435-20806530 | Rare:39 | ||||
chr16:21953009-21953419 | Common:1; Rare:101; Clinvar (benign):3 | ||||
chr16:22436942-22437106 | Rare:60 | ||||
chr16:22437163-22437313 | Rare:45 | ||||
chr16:23453163-23453221 | Rare:16 |