Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:3382081-3382374 | Common:2; Rare:83 | ||||
chr19:3977214-3977633 | Common:4; Rare:140; Clinvar (benign):8 | ||||
chr19:3980513-3980929 | Common:1; Rare:150; Clinvar:3; Clinvar (benign):2 | ||||
chr19:4035831-4035931 | Common:10; Rare:14 | ||||
chr19:4681652-4681834 | Rare:32 | ||||
chr19:5205978-5206162 | Common:6; Rare:37 | ||||
chr19:5229364-5229693 | Common:3; Rare:123 | ||||
chr19:6742746-6743224 | Common:2; Rare:139 | ||||
chr19:6926143-6926408 | Common:8; Rare:63 | ||||
chr19:8394868-8394999 | Rare:32 | ||||
chr19:8423969-8424190 | Common:4; Rare:41 | ||||
chr19:8473678-8473971 | Common:2; Rare:55 | ||||
chr19:8609728-8610037 | Rare:62 | ||||
chr19:8640387-8640408 | Rare:3 | ||||
chr19:11437923-11438124 | Rare:70; Clinvar:1; Clinvar (pathogenic):1 |