Variant report

Variant	rs7731333
Chromosome Location	chr5:113641956-113641957
allele	A/T
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:18)

rs_ID	r²[population]
rs10061203	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11241273	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1124188	0.96[ASN][1000 genomes]
rs12654468	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28446249	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56398861	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs566336	0.84[ASN][1000 genomes]
rs67027308	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs672894	0.84[ASN][1000 genomes]
rs685193	0.83[ASN][1000 genomes]
rs6874042	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6895526	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6897769	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7706180	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7722174	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9326921	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9326922	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9326924	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024203	chr5:113596392-113659935	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1021335	chr5:113599444-113659146	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv537866	chr5:113599444-113659146	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113637400-113643800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:113640800-113642000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr5:113641000-113642000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:113641200-113642000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:113641400-113642800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr5:113641400-113642800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr5:113641400-113643000	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr5:113641400-113643800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:113641400-113643800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr5:113641600-113644000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr5:113641800-113643000	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr5:113641800-113643000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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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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