Variant report

Variant	rs932741
Chromosome Location	chr6:50055171-50055172
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs12213027	1.00[CHB][hapmap];0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs1555679	1.00[ASN][1000 genomes]
rs1575590	1.00[ASN][1000 genomes]
rs57851256	1.00[ASN][1000 genomes]
rs613497	0.86[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs614058	0.90[CEU][hapmap];0.86[YRI][hapmap]
rs638963	0.86[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs6905702	0.88[CEU][hapmap];0.86[YRI][hapmap]
rs6916616	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73739923	1.00[ASN][1000 genomes]
rs73739931	1.00[ASN][1000 genomes]
rs73739932	1.00[ASN][1000 genomes]
rs73739933	1.00[ASN][1000 genomes]
rs73739934	1.00[ASN][1000 genomes]
rs7764678	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9395549	1.00[ASN][1000 genomes]
rs9473708	0.81[AFR][1000 genomes];0.90[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:50054200-50056200	Enhancers	Muscle Satellite Cultured Cells	--
2	chr6:50054200-50056600	Enhancers	HSMM	muscle
3	chr6:50054600-50055200	Enhancers	Fetal Heart	heart
4	chr6:50054600-50056400	Enhancers	HSMMtube	muscle
5	chr6:50054800-50055800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:50054800-50055800	Enhancers	HMEC	breast
7	chr6:50054800-50056000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr6:50055000-50055600	Enhancers	NHEK	skin

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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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