Variant report

Variant rs186497637
Chromosome Location chrX:109928095-109928096
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chrX:109910800-109936600 Weak transcription Primary hematopoietic stem cells blood
2 chrX:109919400-109938200 Weak transcription Cortex derived primary cultured neurospheres brain
3 chrX:109919400-109948800 Weak transcription Adipose Nuclei Adipose
4 chrX:109925400-109931200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chrX:109926000-109928200 Enhancers iPS-18 Cell Line embryonic stem cell
6 chrX:109926200-109928200 Enhancers ES-I3 Cell Line embryonic stem cell
7 chrX:109926800-109928200 Enhancers iPS-15b Cell Line embryonic stem cell
8 chrX:109927600-109928200 Enhancers HUES6 Cell Line embryonic stem cell
9 chrX:109927800-109928200 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
10 chrX:109927800-109928200 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chrX:109928000-109931800 Weak transcription H9 Cell Line embryonic stem cell

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