Variant report

Variant	rs9463016
Chromosome Location	chr6:44709871-44709872
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1000599	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2093346	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs227853	0.81[YRI][hapmap]
rs56793534	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6905609	1.00[EUR][1000 genomes]
rs6926912	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73734734	1.00[EUR][1000 genomes]
rs73734736	1.00[EUR][1000 genomes]
rs73734737	1.00[EUR][1000 genomes]
rs7770848	1.00[EUR][1000 genomes]
rs7775570	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9472333	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9689949	1.00[EUR][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44706600-44710400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr6:44706800-44710400	Weak transcription	Duodenum Mucosa	Duodenum
3	chr6:44707600-44710000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr6:44707800-44710000	Weak transcription	Fetal Intestine Small	intestine
5	chr6:44708000-44710000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:44708000-44710000	Weak transcription	Fetal Intestine Large	intestine
7	chr6:44709600-44710000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr6:44709800-44710800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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