Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:74096975-74097248 | Common:1; Rare:44; Clinvar (benign):1 | ||||
chr10:74100692-74101004 | Rare:66; Clinvar:4; Clinvar (benign):1 | ||||
chr10:74103376-74103660 | Rare:40 | ||||
chr10:74104156-74104258 | Rare:26 | ||||
chr10:74109913-74110230 | Common:3; Rare:49 | ||||
chr10:74112507-74112713 | Rare:36 | ||||
chr10:74112962-74113633 | Common:5; Rare:112 | ||||
chr10:74113940-74114162 | Common:3; Rare:46 | ||||
chr10:74126289-74126444 | Rare:40 | ||||
chr10:74149808-74150085 | Common:3; Rare:38 | ||||
chr10:74224174-74224521 | Common:1; Rare:66 | ||||
chr10:74228176-74228369 | Common:1; Rare:30 | ||||
chr10:74543226-74543277 | Rare:4 | ||||
chr10:74631363-74631407 | Rare:4 | ||||
chr10:74715416-74715496 | Rare:8 |