Variant report

Variant	rs591724
Chromosome Location	chr11:94265772-94265773
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs2508781	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2508783	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs489333	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs528193	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs538800	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs557888	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs560190	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs563882	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs587667	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs588774	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs595672	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:94246000-94267400	Weak transcription	Aorta	Aorta
2	chr11:94259600-94266600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr11:94260200-94268800	Weak transcription	Fetal Intestine Small	intestine
4	chr11:94260600-94269400	Weak transcription	Osteobl	bone
5	chr11:94262600-94266200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr11:94262600-94269600	Weak transcription	HSMMtube	muscle
7	chr11:94265000-94266800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr11:94265200-94266400	Weak transcription	Stomach Mucosa	stomach
9	chr11:94265600-94266400	Weak transcription	Rectal Mucosa Donor 31	rectum

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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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