Variant report

Variant	rs11781413
Chromosome Location	chr8:63445919-63445920
allele	G/T
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:8)

rs_ID	r²[population]
rs11775866	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11781764	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11786601	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11787517	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17835066	0.82[AMR][1000 genomes]
rs1839875	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56121078	0.82[AMR][1000 genomes]
rs6991837	0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv831339	chr8:63312449-63501127	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63442000-63446000	Enhancers	Muscle Satellite Cultured Cells	--
2	chr8:63442400-63446600	Weak transcription	Fetal Brain Male	brain
3	chr8:63443200-63446200	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr8:63443200-63448200	Weak transcription	Fetal Intestine Large	intestine
5	chr8:63443600-63446200	Weak transcription	Pancreas	Pancrea
6	chr8:63444000-63447000	Enhancers	Brain Germinal Matrix	brain
7	chr8:63444600-63449400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr8:63444800-63458200	Weak transcription	Fetal Brain Female	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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