Variant report

Variant	rs62057578
Chromosome Location	chr16:59578174-59578175
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs2406764	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62057572	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62057573	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62057574	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62057575	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62057577	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62057579	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62057580	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62057581	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62057582	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62057583	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62057584	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7185029	0.82[AMR][1000 genomes];0.99[EUR][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	nsv906747	chr16:59385832-60172030	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv916423	chr16:59411801-59750824	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:59575200-59581400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr16:59576200-59580000	Enhancers	HSMM	muscle
3	chr16:59576800-59578400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr16:59577000-59579800	Enhancers	NH-A	brain
5	chr16:59577200-59578200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr16:59577200-59578800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr16:59577400-59578200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr16:59577600-59578200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr16:59577600-59580000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr16:59577800-59578800	Enhancers	NHDF-Ad	bronchial

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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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