Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:14529242-14529635 | Common:1; Rare:154 | ||||
chr19:16572373-16572620 | Common:5; Rare:106 | ||||
chr19:17405587-17405674 | Common:1; Rare:20 | ||||
chr19:17511473-17511673 | Common:3; Rare:87 | ||||
chr19:18919335-18919794 | Common:3; Rare:176 | ||||
chr19:19033484-19033610 | Common:2; Rare:44 | ||||
chr19:19192115-19192268 | Common:1; Rare:50 | ||||
chr19:19192590-19192998 | Common:3; Rare:103; Clinvar (benign):1 | ||||
chr19:19516163-19516247 | Rare:42 | ||||
chr19:29213135-29213234 | Common:1; Rare:38 | ||||
chr19:29606185-29606313 | Rare:42 | ||||
chr19:29665253-29665508 | Common:4; Rare:92 | ||||
chr19:32692269-32692390 | Common:1; Rare:72 | ||||
chr19:32972022-32972242 | Common:3; Rare:53 | ||||
chr19:33521739-33521948 | Rare:71; Clinvar:5 |