Variant report

Variant	rs1034574
Chromosome Location	chr7:104120446-104120447
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10216261	0.96[CEU][hapmap]
rs10234384	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11520992	0.84[CHB][hapmap];0.82[JPT][hapmap]
rs11772914	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11972050	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12705219	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17137948	0.86[JPT][hapmap]
rs6465992	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6961457	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6965697	0.86[JPT][hapmap]
rs7776632	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

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	nsv888925	chr7:104047599-104170560	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104120400-104121600	Bivalent Enhancer	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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