Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:37219076-37219121 | Rare:7 | ||||
chr19:37251632-37251956 | Common:6; Rare:86 | ||||
chr19:37293598-37293647 | |||||
chr19:37304333-37304455 | Common:3; Rare:75 | ||||
chr19:37403869-37404126 | Common:1; Rare:43 | ||||
chr19:37548832-37548994 | Common:1; Rare:58 | ||||
chr19:37790794-37790991 | Rare:29 | ||||
chr19:37853525-37853607 | Rare:10 | ||||
chr19:37855216-37855343 | Common:1; Rare:51 | ||||
chr19:38034445-38034535 | Rare:17 | ||||
chr19:38375929-38376076 | Rare:29 | ||||
chr19:38497202-38497336 | Common:4; Rare:44 | ||||
chr19:38705952-38706130 | Common:2; Rare:29; Clinvar:1; Clinvar (benign):3 | ||||
chr19:38716862-38717316 | Common:2; Rare:96; Clinvar (benign):2 | ||||
chr19:38717735-38717963 | Rare:50; Clinvar (benign):1 |