Variant report

Variant rs73881916
Chromosome Location chr22:33332388-33332389
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:33314000-33380800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr22:33319200-33333000 Weak transcription Fetal Brain Male brain
3 chr22:33327600-33332600 Weak transcription iPS-20b Cell Line embryonic stem cell
4 chr22:33328600-33335400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr22:33328800-33334600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr22:33329000-33333400 Weak transcription HUES64 Cell Line embryonic stem cell
7 chr22:33329200-33336000 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr22:33329400-33333400 Weak transcription H1 Cell Line embryonic stem cell
9 chr22:33331400-33342800 Weak transcription Fetal Heart heart
10 chr22:33332200-33332400 Enhancers Placenta Amnion Placenta Amnion
11 chr22:33332200-33332600 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
12 chr22:33332200-33332600 Enhancers HepG2 liver

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