Variant report

Variant	rs7937659
Chromosome Location	chr11:45780075-45780076
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11038633	0.92[JPT][hapmap]
rs11038645	0.93[ASN][1000 genomes]
rs11038646	0.92[CHB][hapmap];0.86[JPT][hapmap];0.93[ASN][1000 genomes]
rs11038647	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12286489	0.84[CHB][hapmap];0.88[JPT][hapmap];0.91[ASN][1000 genomes]
rs12291983	0.89[ASN][1000 genomes]
rs12295599	0.83[CHB][hapmap];0.89[ASN][1000 genomes]
rs12365302	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1530634	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16938361	0.89[ASN][1000 genomes]
rs2593739	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2666922	1.00[CEU][hapmap];0.83[CHB][hapmap];0.86[JPT][hapmap];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34061867	0.94[ASN][1000 genomes]
rs34462032	0.93[ASN][1000 genomes]
rs35133667	0.89[ASN][1000 genomes]
rs35795927	0.93[ASN][1000 genomes]
rs35997126	0.93[ASN][1000 genomes]
rs3740704	1.00[CEU][hapmap];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7941885	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45775600-45780800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:45777400-45787600	Weak transcription	Right Atrium	heart
3	chr11:45777600-45781800	Weak transcription	Fetal Brain Female	brain

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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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