Variant report

Variant	rs4702098
Chromosome Location	chr5:15671393-15671394
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10053108	0.89[CEU][hapmap];0.83[CHB][hapmap]
rs11745041	0.92[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11953541	0.93[CEU][hapmap]
rs12055198	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12652447	0.89[YRI][hapmap]
rs12654662	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12655307	0.83[CHB][hapmap]
rs12656882	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12658046	1.00[CEU][hapmap];0.86[CHB][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12658048	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12757	0.92[CEU][hapmap]
rs13159972	0.88[CEU][hapmap];0.91[CHB][hapmap];0.85[JPT][hapmap];0.87[ASN][1000 genomes]
rs13165880	0.89[CEU][hapmap];0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs13170478	0.88[CEU][hapmap]
rs13185548	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1429032	0.82[CEU][hapmap]
rs17523312	0.89[CEU][hapmap]
rs17647599	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17703964	0.91[CHB][hapmap]
rs17703976	0.86[CHB][hapmap]
rs1835128	0.81[CEU][hapmap]
rs1835129	0.82[CEU][hapmap]
rs1991529	0.88[CEU][hapmap];0.81[JPT][hapmap]
rs2217346	0.80[CEU][hapmap];0.82[CHB][hapmap]
rs34341354	0.82[CEU][hapmap];0.93[YRI][hapmap]
rs4256343	0.81[YRI][hapmap]
rs4295390	0.92[CEU][hapmap]
rs4702090	0.85[CEU][hapmap];0.83[CHB][hapmap];0.86[JPT][hapmap];0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs58080135	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6869226	0.93[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6873476	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6878081	0.82[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap]
rs6878131	0.92[CEU][hapmap];0.91[CHB][hapmap];0.85[JPT][hapmap];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6891138	0.88[CEU][hapmap];0.81[JPT][hapmap]
rs6895158	0.87[AMR][1000 genomes]
rs6898779	0.92[CEU][hapmap];0.91[CHB][hapmap];0.85[JPT][hapmap];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7701322	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7720476	0.92[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv516929	chr5:15087791-15870300	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1023068	chr5:15095221-15863583	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv869040	chr5:15097602-15866117	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv530222	chr5:15151662-15851485	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv830214	chr5:15589809-15791032	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	esv3507774	chr5:15593461-15822407	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	esv3507776	chr5:15593461-15822407	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1028089	chr5:15636285-15883910	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv537676	chr5:15636285-15883910	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv1024248	chr5:15638067-15863583	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv537677	chr5:15638067-15863583	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv880755	chr5:15670377-15938553	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:15665200-15680800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:15665400-15674400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr5:15667800-15676000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr5:15668400-15674200	Weak transcription	Ovary	ovary
5	chr5:15668400-15679000	Weak transcription	Brain Anterior Caudate	brain
6	chr5:15668600-15673400	Weak transcription	Fetal Heart	heart
7	chr5:15670200-15676000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr5:15670400-15683200	Weak transcription	HUVEC	blood vessel
9	chr5:15671000-15671400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr5:15671000-15671600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr5:15671000-15671800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr5:15671000-15672200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr5:15671000-15672400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr5:15671200-15671600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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