Variant report

Variant	rs71555257
Chromosome Location	chr6:75176533-75176534
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs13193570	0.83[AMR][1000 genomes]
rs13196531	0.83[AMR][1000 genomes]
rs13196893	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13212917	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13216349	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs16884759	0.83[AMR][1000 genomes]
rs34952449	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs34984274	0.83[AMR][1000 genomes]
rs35307888	0.83[AMR][1000 genomes]
rs35756548	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs36053338	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41360849	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71555246	0.83[AMR][1000 genomes]
rs7768066	0.83[AMR][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75175800-75177800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:75176000-75176800	ZNF genes & repeats	Lung	lung
3	chr6:75176000-75177000	Enhancers	Gastric	stomach
4	chr6:75176000-75177800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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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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