Variant report

Variant	rs61115650
Chromosome Location	chr10:50854561-50854562
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10399986	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10400026	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10400027	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10400043	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10400097	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10400098	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10400121	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10400152	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10400162	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10400182	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59551969	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60626181	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60959867	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61132699	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7073028	0.80[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895375	chr10:50306386-51028871	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	esv3346476	chr10:50610853-50987802	Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	esv3385048	chr10:50610942-50988537	Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
4	nsv1037405	chr10:50800817-50940545	Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv895378	chr10:50801342-50955649	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50847000-50860600	Weak transcription	Right Atrium	heart
2	chr10:50852200-50855200	Enhancers	Placenta	Placenta
3	chr10:50853200-50856000	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr10:50853600-50854600	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr10:50853800-50854600	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr10:50854200-50854800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr10:50854200-50854800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr10:50854200-50855000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr10:50854200-50855000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr10:50854400-50854600	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
11	chr10:50854400-50854600	Bivalent Enhancer	NHEK	skin
12	chr10:50854400-50854800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr10:50854400-50854800	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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