Variant report

Variant	rs11155286
Chromosome Location	chr6:143601014-143601015
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11155285	0.90[CHD][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs11155287	0.95[CEU][hapmap];0.82[CHD][hapmap];0.95[JPT][hapmap]
rs11757344	0.90[CHD][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs12526051	0.81[CHD][hapmap];0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs12529438	0.90[JPT][hapmap]
rs892713	0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs9285499	1.00[CEU][hapmap];0.90[TSI][hapmap];0.94[EUR][1000 genomes]
rs9399434	1.00[CEU][hapmap];0.86[JPT][hapmap];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9484717	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9496559	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:143570800-143609200	Weak transcription	Fetal Intestine Large	intestine
2	chr6:143583400-143606000	Weak transcription	Fetal Intestine Small	intestine
3	chr6:143583800-143615400	Weak transcription	K562	blood
4	chr6:143589000-143607400	Weak transcription	Aorta	Aorta
5	chr6:143591400-143605200	Weak transcription	Liver	Liver
6	chr6:143592200-143605600	Weak transcription	Adipose Nuclei	Adipose
7	chr6:143593200-143606800	Weak transcription	NHEK	skin
8	chr6:143593400-143607000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr6:143595400-143605400	Weak transcription	HepG2	liver
10	chr6:143595600-143602800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:143598600-143620200	Weak transcription	Brain Angular Gyrus	brain
12	chr6:143600600-143602200	Weak transcription	Fetal Heart	heart
13	chr6:143600600-143609200	Weak transcription	Brain Anterior Caudate	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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