Variant report

Variant	rs11915036
Chromosome Location	chr3:50836911-50836912
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11914934	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs11927030	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs62257803	1.00[AFR][1000 genomes]
rs62257807	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62257814	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62258667	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs62260125	1.00[AFR][1000 genomes]
rs62260128	1.00[AFR][1000 genomes]
rs62260156	1.00[AFR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50826400-50841200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:50834600-50838600	Weak transcription	H9 Cell Line	embryonic stem cell

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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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