Variant report

Variant	rs7098132
Chromosome Location	chr10:49829754-49829755
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs3910912	0.92[YRI][hapmap]
rs4114457	0.86[AFR][1000 genomes]
rs59719366	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59868190	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7077507	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7084382	0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7909038	0.96[YRI][hapmap];0.99[AFR][1000 genomes];0.87[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	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv895372	chr10:49576878-49933488	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49813400-49844200	Weak transcription	Pancreas	Pancrea
2	chr10:49823000-49830800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr10:49823400-49832000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr10:49827600-49831600	Weak transcription	NHDF-Ad	bronchial
5	chr10:49828800-49841400	Weak transcription	Aorta	Aorta
6	chr10:49829000-49831200	Weak transcription	Right Atrium	heart
7	chr10:49829600-49829800	Enhancers	NHEK	skin

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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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