Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:242088461-242088659 | Common:9; Rare:62 | ||||
chr20:2624222-2624480 | Common:1; Rare:57 | ||||
chr20:3200082-3200392 | Common:1; Rare:80 | ||||
chr20:19757482-19757674 | Common:3; Rare:54 | ||||
chr20:19757959-19758276 | Common:4; Rare:112 | ||||
chr20:23085009-23085167 | Common:1; Rare:54 | ||||
chr20:25281738-25282054 | Common:5; Rare:72 | ||||
chr20:25292298-25292530 | Common:1; Rare:109; Clinvar (pathogenic):1 | ||||
chr20:25751087-25751215 | Rare:28 | ||||
chr20:25853996-25854112 | Common:3; Rare:43 | ||||
chr20:29497304-29497413 | |||||
chr20:33850880-33851077 | Rare:47; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr20:34290599-34290759 | Common:2; Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
chr20:35490957-35491051 | Rare:18 | ||||
chr20:35725972-35726224 | Common:4; Rare:62 |