Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:74496039-74496392 | Common:4; Rare:109 | ||||
chr19:571747-572011 | Common:5; Rare:59 | ||||
chr19:572259-572628 | Common:3; Rare:185 | ||||
chr19:797096-797456 | Rare:145 | ||||
chr19:984277-984343 | Rare:18 | ||||
chr19:2328559-2328703 | Common:2; Rare:70 | ||||
chr19:5622746-5623139 | Common:5; Rare:143 | ||||
chr19:5978078-5978364 | Common:3; Rare:106 | ||||
chr19:7395037-7395176 | Common:4; Rare:44 | ||||
chr19:7629528-7629838 | Common:5; Rare:110; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7943644-7944017 | Rare:102 | ||||
chr19:8321324-8321568 | Common:2; Rare:113 | ||||
chr19:8390101-8390411 | Common:1; Rare:92 | ||||
chr19:8444814-8444996 | Common:2; Rare:79 | ||||
chr19:10333517-10333738 | Rare:73 |