Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:2096524-2097046 | Common:1; Rare:175 | ||||
chr19:2163761-2164230 | Common:2; Rare:137 | ||||
chr19:2233999-2234206 | Rare:101 | ||||
chr19:2256425-2256516 | Common:1; Rare:12 | ||||
chr19:2269459-2269859 | Common:6; Rare:186 | ||||
chr19:2328386-2328703 | Common:2; Rare:136 | ||||
chr19:2427441-2427630 | Common:1; Rare:95 | ||||
chr19:2431564-2431855 | Rare:119; Clinvar:2; Clinvar (benign):2 | ||||
chr19:2434412-2434797 | Common:1; Rare:127; Clinvar (benign):2 | ||||
chr19:2456885-2457097 | Rare:61; Clinvar:1 | ||||
chr19:2721342-2721470 | Rare:28 | ||||
chr19:2783224-2783490 | Rare:91 | ||||
chr19:2810149-2810381 | Common:3; Rare:74 | ||||
chr19:2819740-2819999 | Common:4; Rare:69 | ||||
chr19:2977276-2977586 | Common:2; Rare:109 |