Variant report

Variant	rs7631740
Chromosome Location	chr3:159133317-159133318
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs11917412	0.94[CEU][hapmap]
rs11917829	0.94[CEU][hapmap];1.00[CHB][hapmap];0.86[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap]
rs11920486	0.87[CEU][hapmap]
rs12696092	0.93[CEU][hapmap]
rs13061579	0.94[CEU][hapmap]
rs13061619	0.94[CEU][hapmap]
rs13065679	0.94[CEU][hapmap]
rs13066122	0.87[CEU][hapmap]
rs13070853	0.87[CEU][hapmap]
rs13075790	0.93[CEU][hapmap]
rs13077258	0.94[CEU][hapmap]
rs13080892	0.87[CEU][hapmap]
rs13083244	0.94[CEU][hapmap]
rs13083887	0.87[CEU][hapmap]
rs13085008	0.93[CEU][hapmap]
rs13085667	0.94[CEU][hapmap]
rs13091349	0.88[CEU][hapmap]
rs13095658	0.93[CEU][hapmap]
rs1448996	0.94[CEU][hapmap]
rs1449002	0.87[CEU][hapmap]
rs16830135	0.89[CHB][hapmap];0.89[JPT][hapmap]
rs16830184	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16830232	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs16830267	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs16830290	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs16830298	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16830299	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16830314	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16830326	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs16830331	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16830334	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap]
rs17795417	0.93[CEU][hapmap]
rs1839219	0.94[CEU][hapmap]
rs1844468	1.00[CHB][hapmap];0.85[CHD][hapmap];0.88[JPT][hapmap];0.88[ASN][1000 genomes]
rs1906951	0.94[CEU][hapmap]
rs1973660	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2029100	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2029101	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2102724	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2886480	0.93[CEU][hapmap]
rs3912726	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6781001	0.88[CEU][hapmap]
rs6781285	0.87[CEU][hapmap]
rs6784143	0.94[CEU][hapmap]
rs6796565	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7620377	0.94[CEU][hapmap]
rs7620403	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7629397	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7639707	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs7642306	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7644770	0.94[CEU][hapmap]
rs870852	0.87[CEU][hapmap]
rs9848338	0.93[CEU][hapmap]
rs9848831	0.93[CEU][hapmap]
rs9871361	0.88[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530059	chr3:158332590-159147549	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv470971	chr3:158590928-159158217	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	nsv998949	chr3:158774806-159394550	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1004990	chr3:159090974-159174954	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7631740	TRIM59	cis	parietal	SCAN

Chromatin state (count:0 , 50 per page) page:

No data

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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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