Variant report

Variant	rs7136870
Chromosome Location	chr12:104090117-104090118
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10861073	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs11111716	0.82[EUR][1000 genomes]
rs12314920	0.95[CHB][hapmap];0.88[GIH][hapmap];0.86[JPT][hapmap];0.86[MEX][hapmap];0.84[TSI][hapmap]
rs12368532	0.95[CHB][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs1593809	0.95[CHB][hapmap];0.80[JPT][hapmap]
rs4981017	0.95[CHB][hapmap];0.85[JPT][hapmap];0.83[ASN][1000 genomes]
rs4981018	1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs4981031	0.87[CHB][hapmap];0.98[GIH][hapmap];0.91[MEX][hapmap];0.88[AMR][1000 genomes]
rs58605677	0.83[ASN][1000 genomes]
rs697202	1.00[CHB][hapmap];0.97[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7296561	0.82[EUR][1000 genomes]
rs7296691	0.92[CEU][hapmap];0.80[TSI][hapmap];0.82[EUR][1000 genomes]
rs7303939	0.95[CHB][hapmap];0.88[GIH][hapmap];0.91[JPT][hapmap];0.84[TSI][hapmap];0.83[ASN][1000 genomes]
rs7304095	0.95[CHB][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs7312283	0.92[CEU][hapmap];0.81[TSI][hapmap];0.82[EUR][1000 genomes]

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	nsv560038	chr12:104053420-104092996	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7136870	TXNRD1	cis	parietal	SCAN
rs7136870	PAH	cis	cerebellum	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104086000-104091200	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr12:104089400-104090200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
3	chr12:104089800-104093800	Strong transcription	Spleen	Spleen

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Input of quick search could be:

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

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