Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45902577-45902954 | Common:3; Rare:119 | ||||
chr19:45973277-45973685 | Common:1; Rare:54 | ||||
chr19:46346927-46347176 | Common:3; Rare:86 | ||||
chr19:46471437-46471718 | Common:7; Rare:108 | ||||
chr19:46495811-46496030 | Rare:62 | ||||
chr19:46600891-46601434 | Common:6; Rare:188; Clinvar (benign):3 | ||||
chr19:46661025-46661236 | Rare:54 | ||||
chr19:46661349-46661645 | Rare:98 | ||||
chr19:46725330-46725597 | Rare:94 | ||||
chr19:46745853-46746068 | Common:3; Rare:43 | ||||
chr19:46746246-46746681 | Common:4; Rare:114 | ||||
chr19:46746781-46746914 | Rare:20 | ||||
chr19:46746923-46747214 | Rare:50 | ||||
chr19:46850245-46850393 | Rare:21 | ||||
chr19:47112037-47112088 | Common:3; Rare:10 |