Variant report

Variant	rs11850520
Chromosome Location	chr14:63238005-63238006
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11846818	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11850687	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1490029	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs1490030	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs17100383	0.82[YRI][hapmap];0.84[AFR][1000 genomes]
rs7143144	0.84[EUR][1000 genomes]
rs8007544	0.82[YRI][hapmap];0.81[AFR][1000 genomes]
rs8022090	1.00[CEU][hapmap];0.92[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63227200-63246400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:63233200-63248800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr14:63237400-63243200	Weak transcription	Skeletal Muscle Female	skeletal muscle

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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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