Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:136289779-136290014 | Common:1; Rare:102 | ||||
chr6:136550404-136550611 | Common:2; Rare:60 | ||||
chr6:137219356-137219518 | Common:4; Rare:51; Clinvar (benign):2 | ||||
chr6:138773642-138773795 | Common:1; Rare:69 | ||||
chr6:143060742-143060926 | Common:7; Rare:65 | ||||
chr6:143450654-143450884 | Common:1; Rare:95; Clinvar:3; Clinvar (benign):1 | ||||
chr6:145814731-145814920 | Common:1; Rare:91 | ||||
chr6:149749617-149749788 | Rare:95 | ||||
chr6:151452032-151452331 | Common:3; Rare:96 | ||||
chr6:152983009-152983287 | Common:2; Rare:86 | ||||
chr6:157323509-157323580 | Common:2; Rare:28 | ||||
chr6:158168233-158168377 | Common:2; Rare:49 | ||||
chr6:158999761-158999776 | Common:1; Rare:9; Clinvar:1; Clinvar (benign):1 | ||||
chr6:159693265-159693585 | Common:5; Rare:87 | ||||
chr6:159726948-159727155 | Rare:81 |