Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:41239709-41240040 | Common:2; Rare:64 | ||||
chr19:41241135-41241430 | Common:1; Rare:45 | ||||
chr19:41241613-41241797 | Rare:27 | ||||
chr19:41248521-41248826 | Common:2; Rare:82 | ||||
chr19:41252293-41252450 | Rare:50 | ||||
chr19:41265706-41265767 | Rare:11 | ||||
chr19:41325520-41325569 | Rare:9 | ||||
chr19:41331844-41332141 | Rare:60; Clinvar (benign):1 | ||||
chr19:41352763-41352975 | Common:1; Rare:55; Clinvar (benign):1 | ||||
chr19:41862208-41862398 | Common:1; Rare:52 | ||||
chr19:42270469-42270597 | Rare:18 | ||||
chr19:42336839-42337112 | Rare:75; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr19:42396905-42397199 | Common:1; Rare:69 | ||||
chr19:43197232-43197522 | Common:3; Rare:62 | ||||
chr19:43506631-43506733 | Rare:27 |