Variant report

Variant	rs7317488
Chromosome Location	chr13:40379594-40379595
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11617586	0.99[ASN][1000 genomes]
rs12019493	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12020434	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12857806	0.94[ASN][1000 genomes]
rs12859245	0.93[ASN][1000 genomes]
rs34927174	0.89[ASN][1000 genomes]
rs4312181	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4531603	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4943700	0.99[ASN][1000 genomes]
rs7335495	0.99[ASN][1000 genomes]
rs7988955	0.92[ASN][1000 genomes]
rs9594367	0.99[ASN][1000 genomes]
rs9594368	0.98[ASN][1000 genomes]
rs9603618	0.96[ASN][1000 genomes]
rs9603619	0.95[ASN][1000 genomes]
rs9603620	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9603621	0.99[ASN][1000 genomes]
rs9603626	0.99[ASN][1000 genomes]
rs9603627	0.92[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	nsv1054600	chr13:39801283-40545027	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1054797	chr13:40198744-40618428	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
3	nsv541755	chr13:40198744-40618428	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
4	nsv1040458	chr13:40249387-40638129	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:40377200-40380000	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr13:40377200-40380200	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr13:40377400-40380000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr13:40377600-40379800	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr13:40378000-40380000	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr13:40378400-40384200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr13:40379000-40380000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr13:40379200-40380000	Enhancers	H1 Cell Line	embryonic stem cell
9	chr13:40379400-40379800	Enhancers	Placenta	Placenta

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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