Variant report

Variant rs2786609
Chromosome Location chr1:220715278-220715279
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:220703400-220724400 Weak transcription Aorta Aorta
2 chr1:220706000-220723800 Weak transcription Fetal Brain Male brain
3 chr1:220708800-220718000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:220710200-220717800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr1:220713200-220715800 Weak transcription H1 Cell Line embryonic stem cell
6 chr1:220714800-220716200 Enhancers iPS-20b Cell Line embryonic stem cell
7 chr1:220715000-220716200 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr1:220715200-220715400 ZNF genes & repeats Cortex derived primary cultured neurospheres brain
9 chr1:220715200-220715600 Weak transcription ES-I3 Cell Line embryonic stem cell

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