Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:70205664-70205790 | Common:3; Rare:48; Clinvar (benign):2 | ||||
chr19:572289-572603 | Common:3; Rare:153 | ||||
chr19:893177-893484 | Common:3; Rare:131 | ||||
chr19:1103795-1104100 | Common:4; Rare:130 | ||||
chr19:1354735-1354988 | Common:2; Rare:103 | ||||
chr19:2328562-2328696 | Rare:66 | ||||
chr19:4867626-4867853 | Common:3; Rare:68 | ||||
chr19:5622759-5623139 | Common:5; Rare:134 | ||||
chr19:5978089-5978373 | Common:3; Rare:105 | ||||
chr19:7395045-7395163 | Common:2; Rare:35 | ||||
chr19:7629539-7629836 | Common:5; Rare:105; Clinvar (benign):2 | ||||
chr19:8321344-8321544 | Common:2; Rare:91 | ||||
chr19:8363852-8364162 | Common:3; Rare:68 | ||||
chr19:8390048-8390411 | Common:1; Rare:103 | ||||
chr19:9621192-9621525 | Common:3; Rare:92 |