Variant report

Variant	rs377895
Chromosome Location	chr6:147797274-147797275
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs325106	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs387454	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs586354	0.83[EUR][1000 genomes]
rs587008	0.90[ASN][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147796600-147798000	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr6:147797000-147797800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:147797200-147797800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr6:147797200-147797800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr6:147797200-147797800	Enhancers	Brain Hippocampus Middle	brain
6	chr6:147797200-147798000	Enhancers	Brain Substantia Nigra	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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