Variant report

Variant	rs58382291
Chromosome Location	chr7:83785537-83785538
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs17158642	0.91[ASN][1000 genomes]
rs17158647	0.91[ASN][1000 genomes]
rs17158675	1.00[ASN][1000 genomes]
rs17158680	1.00[EUR][1000 genomes]
rs17158685	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28433968	0.91[ASN][1000 genomes]
rs28708904	0.91[ASN][1000 genomes]
rs55923950	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56663012	1.00[EUR][1000 genomes]
rs58675984	1.00[EUR][1000 genomes]
rs58741896	0.91[ASN][1000 genomes]
rs59186128	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60227422	1.00[EUR][1000 genomes]
rs66539631	1.00[EUR][1000 genomes]
rs6943044	1.00[EUR][1000 genomes]
rs6944814	0.91[ASN][1000 genomes]
rs6946101	0.91[ASN][1000 genomes]
rs6966352	1.00[EUR][1000 genomes]
rs6975522	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73177447	0.91[ASN][1000 genomes]
rs73177452	0.91[ASN][1000 genomes]
rs73177461	0.91[ASN][1000 genomes]
rs73177476	0.91[ASN][1000 genomes]
rs73177479	0.91[ASN][1000 genomes]
rs73378880	0.91[ASN][1000 genomes]
rs73378884	0.91[ASN][1000 genomes]
rs73380806	0.91[ASN][1000 genomes]
rs73380837	1.00[ASN][1000 genomes]
rs73380843	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7786079	1.00[EUR][1000 genomes]
rs7786377	1.00[EUR][1000 genomes]
rs7804558	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7806601	1.00[EUR][1000 genomes]
rs7808547	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529344	chr7:83714286-84592857	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv888629	chr7:83722691-83896025	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1017884	chr7:83724138-83972995	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv538995	chr7:83724138-83972995	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv3692934	chr7:83778360-83786460	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv442055	chr7:83782433-83786688	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv519788	chr7:83782435-83786460	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv517852	chr7:83782435-83794756	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv514429	chr7:83782496-83786688	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv888630	chr7:83782839-83809111	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:83770800-83795000	Weak transcription	NHDF-Ad	bronchial
2	chr7:83775400-83791600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:83777000-83803000	Weak transcription	NHLF	lung
4	chr7:83778000-83803000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:83779400-83791600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:83780000-83786200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr7:83780000-83786400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:83780000-83786400	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr7:83780000-83786600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr7:83780200-83786600	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr7:83783000-83788800	Weak transcription	Fetal Heart	heart
12	chr7:83784200-83786600	Enhancers	Rectal Smooth Muscle	rectum
13	chr7:83784200-83787200	Enhancers	Fetal Lung	lung
14	chr7:83784800-83786200	Weak transcription	Colon Smooth Muscle	Colon
15	chr7:83784800-83787000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:83785000-83786600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr7:83785000-83789000	Weak transcription	Stomach Smooth Muscle	stomach
18	chr7:83785000-83791600	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr7:83785000-83803000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr7:83785200-83790600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:83785200-83790800	Weak transcription	Fetal Stomach	stomach

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