Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:4767114-4767296 | Common:2; Rare:64 | ||||
chr16:4802838-4803099 | Common:3; Rare:124; Clinvar:3; Clinvar (benign):1 | ||||
chr16:5033920-5034010 | Rare:32 | ||||
chr16:5071778-5071872 | Rare:48; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr16:5097726-5098007 | Common:4; Rare:104 | ||||
chr16:6018720-6019235 | Rare:165 | ||||
chr16:6019435-6019602 | Common:1; Rare:55 | ||||
chr16:6019605-6019941 | Rare:132; Clinvar:1 | ||||
chr16:8674439-8674666 | Common:1; Rare:80; Clinvar:2 | ||||
chr16:8712595-8713379 | Common:7; Rare:168 | ||||
chr16:8713841-8713947 | Rare:38 | ||||
chr16:8720534-8720782 | Common:2; Rare:70 | ||||
chr16:8797595-8797877 | Common:1; Rare:113; Clinvar:2; Clinvar (benign):2 | ||||
chr16:8868977-8869218 | Common:3; Rare:114 | ||||
chr16:10743699-10743882 | Rare:79 |