Variant report

Variant	rs4610188
Chromosome Location	chr3:28642854-28642855
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs4133027	0.83[ASN][1000 genomes]
rs4234338	0.85[CEU][hapmap];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4234339	0.81[CEU][hapmap];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4234340	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4234341	0.90[CEU][hapmap];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4356777	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4368456	0.90[CEU][hapmap];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4478040	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4521182	0.90[ASN][1000 genomes]
rs4522734	0.88[ASN][1000 genomes]
rs4680762	0.81[EUR][1000 genomes]
rs6549860	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6549861	0.90[ASN][1000 genomes]
rs6789363	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6796390	0.92[ASN][1000 genomes]
rs7619927	0.83[ASN][1000 genomes]
rs7642049	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7643191	0.80[CEU][hapmap]
rs9815067	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3328565	chr3:27991169-28915035	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv876649	chr3:28126595-28718454	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1015015	chr3:28461972-28728494	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv916364	chr3:28468275-29146280	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv590010	chr3:28469830-28727214	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv524090	chr3:28631124-28645278	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:28642400-28643000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:28642400-28643200	Enhancers	Pancreas	Pancrea
3	chr3:28642600-28643000	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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