Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:1103801-1104114 | Common:4; Rare:131 | ||||
chr19:1275788-1276112 | Common:2; Rare:143 | ||||
chr19:2015395-2015538 | Rare:53 | ||||
chr19:2096257-2096415 | Rare:54 | ||||
chr19:2328516-2328707 | Common:2; Rare:98 | ||||
chr19:5622765-5623139 | Common:5; Rare:132 | ||||
chr19:5978078-5978348 | Common:3; Rare:102 | ||||
chr19:6740819-6740931 | Rare:26 | ||||
chr19:7535574-7535744 | Common:3; Rare:56 | ||||
chr19:7629539-7629826 | Common:5; Rare:101; Clinvar (benign):1 | ||||
chr19:7636993-7637181 | Common:2; Rare:58; Clinvar (benign):1 | ||||
chr19:8308299-8308638 | Common:2; Rare:107 | ||||
chr19:8321336-8321653 | Common:2; Rare:137 | ||||
chr19:8390073-8390419 | Common:1; Rare:99 | ||||
chr19:8413031-8413360 | Common:5; Rare:134 |