Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:4831701-4832044 | Common:3; Rare:65 | ||||
chr19:4867621-4867932 | Common:4; Rare:91 | ||||
chr19:5622740-5623181 | Common:5; Rare:168 | ||||
chr19:5680941-5681030 | Rare:23 | ||||
chr19:6110516-6110834 | Common:2; Rare:98 | ||||
chr19:6393385-6393580 | Common:2; Rare:58 | ||||
chr19:6684773-6685069 | Rare:82; Clinvar (benign):1 | ||||
chr19:7395057-7395179 | Common:3; Rare:38 | ||||
chr19:7629524-7629836 | Common:5; Rare:111; Clinvar (benign):2 | ||||
chr19:8321347-8321560 | Common:2; Rare:94 | ||||
chr19:8363959-8364183 | Common:2; Rare:57 | ||||
chr19:8390062-8390411 | Common:1; Rare:98 | ||||
chr19:8444791-8444996 | Common:4; Rare:89 | ||||
chr19:9538603-9538716 | Common:1; Rare:33 | ||||
chr19:9621192-9621500 | Common:3; Rare:86 |