Variant report

Variant	rs575175
Chromosome Location	chr3:23019664-23019665
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs680110	0.80[ASN][1000 genomes]
rs822773	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014828	chr3:22554271-23033498	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1008306	chr3:22762892-23026548	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23016600-23021000	Weak transcription	Ovary	ovary
2	chr3:23018800-23021000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:23019200-23024800	Enhancers	Fetal Heart	heart
4	chr3:23019400-23020000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr3:23019400-23021400	Enhancers	Left Ventricle	heart
6	chr3:23019600-23020600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr3:23019600-23021200	Weak transcription	Lung	lung
8	chr3:23019600-23022000	Weak transcription	Skeletal Muscle Female	skeletal muscle

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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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