Variant report

Variant	rs6857403
Chromosome Location	chr4:82079789-82079790
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10002599	0.81[AMR][1000 genomes]
rs10003341	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10005912	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10516650	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11099460	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11722020	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11933194	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11941219	0.81[AMR][1000 genomes]
rs12330930	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12331759	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12331821	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12332035	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12643702	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12651341	0.84[EUR][1000 genomes]
rs1517547	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1545287	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1546651	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1972127	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2028642	0.82[EUR][1000 genomes]
rs28413060	0.81[AMR][1000 genomes]
rs28445932	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28491787	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28508156	0.81[AMR][1000 genomes]
rs28669195	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2868141	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28782932	0.81[AMR][1000 genomes]
rs28783134	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28844140	0.81[AMR][1000 genomes]
rs2903751	0.86[AMR][1000 genomes]
rs3733550	0.84[EUR][1000 genomes]
rs3943629	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4566647	0.84[EUR][1000 genomes]
rs56008646	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs59896344	0.80[EUR][1000 genomes]
rs60111302	0.80[EUR][1000 genomes]
rs60808851	0.81[AMR][1000 genomes]
rs6811913	0.81[AMR][1000 genomes]
rs6828114	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6848802	0.87[EUR][1000 genomes]
rs72878860	0.84[EUR][1000 genomes]
rs72879491	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72879493	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72879502	0.86[AMR][1000 genomes]
rs72880604	0.80[EUR][1000 genomes]
rs72881305	0.86[AMR][1000 genomes]
rs7687258	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs986290	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9990953	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999729	chr4:81802554-82627820	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537156	chr4:81802554-82627820	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv829984	chr4:81979988-82113977	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
4	esv1822437	chr4:82025743-82118996	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	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	chr4:82071000-82085400	Weak transcription	NHDF-Ad	bronchial
2	chr4:82075200-82085400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:82075400-82081200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:82075400-82082800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr4:82075400-82083400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:82075400-82083600	Weak transcription	Fetal Intestine Large	intestine
7	chr4:82075400-82085800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr4:82079200-82085400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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