Variant report

Variant	rs62306419
Chromosome Location	chr4:63008418-63008419
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10014304	1.00[ASN][1000 genomes]
rs10517557	1.00[ASN][1000 genomes]
rs10517558	1.00[ASN][1000 genomes]
rs11131360	1.00[ASN][1000 genomes]
rs13108646	1.00[ASN][1000 genomes]
rs13109058	1.00[ASN][1000 genomes]
rs13111304	1.00[ASN][1000 genomes]
rs13118308	1.00[ASN][1000 genomes]
rs13123239	1.00[ASN][1000 genomes]
rs13125062	1.00[ASN][1000 genomes]
rs13131100	1.00[ASN][1000 genomes]
rs13143865	1.00[ASN][1000 genomes]
rs13149735	1.00[ASN][1000 genomes]
rs1350649	1.00[ASN][1000 genomes]
rs1397545	1.00[ASN][1000 genomes]
rs17828666	1.00[ASN][1000 genomes]
rs1870528	1.00[ASN][1000 genomes]
rs28447188	1.00[ASN][1000 genomes]
rs33932625	1.00[ASN][1000 genomes]
rs34978365	1.00[ASN][1000 genomes]
rs4860455	1.00[ASN][1000 genomes]
rs4860459	1.00[ASN][1000 genomes]
rs56150500	1.00[ASN][1000 genomes]
rs67529975	1.00[ASN][1000 genomes]
rs6841045	1.00[ASN][1000 genomes]
rs72641216	1.00[ASN][1000 genomes]
rs9994443	1.00[ASN][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	nsv879078	chr4:62923797-63054757	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv594332	chr4:62976756-63034074	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1005620	chr4:62978115-63035387	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription	TF binding region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1013327	chr4:62989426-63149048	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:63004400-63011200	Weak transcription	Right Ventricle	heart
2	chr4:63005000-63011200	Weak transcription	Left Ventricle	heart
3	chr4:63008000-63008600	Active TSS	Fetal Heart	heart

Quick Search:

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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