Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:11988563-11988728 | Common:1; Rare:37 | ||||
chr19:12797094-12797253 | Rare:36 | ||||
chr19:15191803-15192049 | Common:1; Rare:83; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:19776391-19776586 | Common:2; Rare:52 | ||||
chr19:19861173-19861363 | Rare:31 | ||||
chr19:20238291-20238611 | Common:5; Rare:91 | ||||
chr19:20424830-20425082 | Common:4; Rare:46 | ||||
chr19:20999793-20999967 | Common:4; Rare:54 | ||||
chr19:21447867-21448090 | Common:4; Rare:29 | ||||
chr19:21448976-21449240 | Rare:52 | ||||
chr19:21451910-21452073 | Common:2; Rare:27 | ||||
chr19:21474686-21474883 | Common:4; Rare:61 | ||||
chr19:23274172-23274373 | Common:2; Rare:57 | ||||
chr19:23762848-23763080 | Common:3; Rare:78 | ||||
chr19:27793153-27793479 | Common:5; Rare:78 |