Variant report

Variant	rs4773682
Chromosome Location	chr13:93071380-93071381
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr13:93070548..93072245-chr13:93081774..93084405,2	K562	blood:
2	chr13:93070745..93072680-chr13:93082905..93085536,2	K562	blood:
3	chr13:93053170..93056037-chr13:93069386..93072124,2	K562	blood:

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1023013	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1023014	0.87[ASN][1000 genomes]
rs1926608	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1926609	0.86[ASN][1000 genomes]
rs1926610	0.95[CEU][hapmap];0.93[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2031803	0.92[CEU][hapmap];0.92[EUR][1000 genomes]
rs2104624	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2209836	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2209839	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2209840	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2225158	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2374006	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2374009	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs2888720	0.92[CEU][hapmap];0.82[CHB][hapmap];0.80[JPT][hapmap]
rs4142024	0.87[ASN][1000 genomes]
rs4771859	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs6492607	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs7317952	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7324463	0.82[CHB][hapmap]
rs7329553	0.82[CHB][hapmap]
rs7988626	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7996390	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9516072	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][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	esv2756005	chr13:92584199-93080799	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv832680	chr13:93021114-93181489	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93071000-93071600	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr13:93071000-93072400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr13:93071200-93071400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:93071200-93071600	Enhancers	Fetal Intestine Large	intestine
5	chr13:93071200-93071600	Enhancers	Stomach Mucosa	stomach

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