Variant report

Variant	rs4731194
Chromosome Location	chr7:124285988-124285989
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10253582	0.84[EUR][1000 genomes]
rs10264807	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10265015	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10266863	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10954042	0.82[EUR][1000 genomes]
rs11977720	0.84[EUR][1000 genomes]
rs13228817	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13245806	0.80[EUR][1000 genomes]
rs1404404	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1524757	0.82[EUR][1000 genomes]
rs1540830	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1917361	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1917362	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2049438	0.90[EUR][1000 genomes]
rs2049439	0.90[EUR][1000 genomes]
rs2204380	0.91[EUR][1000 genomes]
rs2204381	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34541525	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7784041	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv429809	chr7:123937674-124835925	Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
2	nsv831118	chr7:124172267-124347527	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124271400-124287600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:124283400-124287200	Weak transcription	Brain Angular Gyrus	brain
3	chr7:124284600-124287600	Weak transcription	Fetal Lung	lung
4	chr7:124284800-124289000	Weak transcription	Brain Cingulate Gyrus	brain
5	chr7:124285200-124289400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr7:124285600-124286200	Enhancers	Brain Hippocampus Middle	brain

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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