Variant report

Variant	rs73144888
Chromosome Location	chr5:92390314-92390315
allele	C/T
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:11)

rs_ID	r²[population]
rs10514367	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67632512	1.00[ASN][1000 genomes]
rs67776649	1.00[ASN][1000 genomes]
rs68019574	1.00[ASN][1000 genomes]
rs6863272	1.00[ASN][1000 genomes]
rs6887432	1.00[ASN][1000 genomes]
rs72784417	1.00[ASN][1000 genomes]
rs73144883	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73144886	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7706380	1.00[ASN][1000 genomes]
rs7732043	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	nsv1015770	chr5:91911877-92498264	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1022712	chr5:92191693-92415111	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1028930	chr5:92194772-92415111	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv830399	chr5:92290915-92462490	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	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	chr5:92388200-92390400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:92389200-92390600	Enhancers	HepG2	liver
3	chr5:92389200-92391400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:92389400-92391200	Enhancers	Muscle Satellite Cultured Cells	--
5	chr5:92389600-92390600	Enhancers	A549	lung
6	chr5:92389600-92391000	Enhancers	NHLF	lung
7	chr5:92389800-92391200	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr5:92389800-92393000	Weak transcription	NHDF-Ad	bronchial
9	chr5:92390200-92390600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr5:92390200-92390800	Enhancers	Osteobl	bone

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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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