Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:40717156-40717397 | Common:1; Rare:80 | ||||
chr19:40718056-40718288 | Rare:77 | ||||
chr19:40750588-40750909 | Common:2; Rare:67 | ||||
chr19:40751080-40751249 | Common:1; Rare:47 | ||||
chr19:41219105-41219475 | Common:1; Rare:103 | ||||
chr19:41264752-41265143 | Common:2; Rare:88 | ||||
chr19:41363794-41363992 | Common:1; Rare:70; Clinvar:1 | ||||
chr19:41364123-41364211 | Rare:30; Clinvar:1 | ||||
chr19:41397324-41397605 | Common:4; Rare:73 | ||||
chr19:41860080-41860289 | Common:1; Rare:84; Clinvar:3; Clinvar (benign):1 | ||||
chr19:41884122-41884437 | Rare:76 | ||||
chr19:42070138-42070331 | Rare:54 | ||||
chr19:42075809-42076209 | Rare:114 | ||||
chr19:42132430-42132622 | Rare:36 | ||||
chr19:42220120-42220358 | Common:2; Rare:64 |