Variant report

Variant	rs7097017
Chromosome Location	chr10:4333424-4333425
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10904223	0.92[EUR][1000 genomes]
rs10904224	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11252445	0.93[EUR][1000 genomes]
rs1923395	0.80[GIH][hapmap]
rs1923397	0.80[GIH][hapmap]
rs7916188	0.83[EUR][1000 genomes]
rs9423525	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9423526	0.83[AMR][1000 genomes];0.92[EUR][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	nsv894785	chr10:4306421-4372629	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv518582	chr10:4328928-4336606	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4327000-4334600	Weak transcription	Right Atrium	heart
2	chr10:4327800-4334200	Weak transcription	NHDF-Ad	bronchial
3	chr10:4331200-4338200	Weak transcription	Brain Germinal Matrix	brain
4	chr10:4332800-4334200	Weak transcription	Fetal Brain Female	brain
5	chr10:4333200-4334800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr10:4333400-4334400	Weak transcription	Fetal Brain Male	brain

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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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