Variant report

Variant	rs71472823
Chromosome Location	chr10:22771852-22771853
allele	-/A
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv982870	chr10:22770802-22778774	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:22765800-22806600	Weak transcription	Right Atrium	heart
2	chr10:22771000-22772200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:22771000-22772200	Enhancers	GM12878-XiMat	blood
4	chr10:22771000-22780200	Weak transcription	Brain Angular Gyrus	brain
5	chr10:22771200-22772000	Enhancers	Stomach Mucosa	stomach
6	chr10:22771200-22772800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr10:22771400-22775600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr10:22771600-22775200	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr10:22771600-22779800	Weak transcription	Brain Substantia Nigra	brain
10	chr10:22771800-22775200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr10:22771800-22778400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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