Variant report

Variant	rs7170335
Chromosome Location	chr15:39938085-39938086
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:39936644..39939290-chr15:39941408..39943879,2	K562	blood:

Extended variants
information (count: 101 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs10152640	0.84[CHB][hapmap];0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs10520137	0.80[CHB][hapmap]
rs10520138	0.80[CHB][hapmap];0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs10520142	0.94[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.95[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11070222	0.80[CHB][hapmap]
rs11070226	0.89[ASN][1000 genomes]
rs11070227	0.89[ASN][1000 genomes]
rs11070228	0.89[ASN][1000 genomes]
rs11630406	0.90[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs11631820	0.83[YRI][hapmap]
rs11631824	0.83[YRI][hapmap]
rs11632117	0.92[ASN][1000 genomes]
rs11632879	0.90[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs11635103	0.90[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs11636823	0.92[ASN][1000 genomes]
rs11638041	0.89[ASN][1000 genomes]
rs11638558	0.89[ASN][1000 genomes]
rs11852591	0.90[CHB][hapmap];0.90[JPT][hapmap];0.88[ASN][1000 genomes]
rs11852649	0.90[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs11855487	0.89[ASN][1000 genomes]
rs11856971	0.90[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs12050804	0.86[YRI][hapmap]
rs12443011	0.85[CHB][hapmap];0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs12908846	0.80[CHB][hapmap]
rs1478605	0.84[CHB][hapmap]
rs16969386	0.80[CHB][hapmap]
rs16969395	0.80[ASN][1000 genomes]
rs16969410	0.80[CHB][hapmap]
rs16969426	0.89[ASN][1000 genomes]
rs16969429	0.89[ASN][1000 genomes]
rs16969451	0.89[ASN][1000 genomes]
rs16969459	0.90[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs16969475	0.95[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs16969478	0.95[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs1876852	1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[YRI][hapmap];0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1876853	0.95[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs2411300	0.86[EUR][1000 genomes]
rs2411310	0.95[YRI][hapmap]
rs2411313	0.90[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs2411314	0.89[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs2411315	0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.89[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2412412	1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[YRI][hapmap];0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2412413	0.95[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs2412414	0.89[ASN][1000 genomes]
rs2412415	0.90[CHB][hapmap];0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs2412416	0.89[ASN][1000 genomes]
rs2412417	0.90[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs2412418	0.95[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2412419	0.80[CHB][hapmap]
rs2898686	0.90[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs2898687	0.95[CHB][hapmap];0.89[JPT][hapmap]
rs2898688	0.90[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs2898962	0.89[ASN][1000 genomes]
rs4319738	0.82[AFR][1000 genomes]
rs4319740	0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4349120	0.90[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs4479205	0.89[ASN][1000 genomes]
rs4493017	0.95[YRI][hapmap];0.81[AFR][1000 genomes]
rs4526992	0.91[ASN][1000 genomes]
rs4547308	0.90[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs4583211	0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs4628934	0.89[ASN][1000 genomes]
rs59449051	0.92[ASN][1000 genomes]
rs60164392	0.89[ASN][1000 genomes]
rs60195210	0.89[ASN][1000 genomes]
rs61130460	0.90[ASN][1000 genomes]
rs61439563	0.92[ASN][1000 genomes]
rs61568256	0.90[ASN][1000 genomes]
rs6492911	0.81[YRI][hapmap]
rs66781090	0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7162070	0.95[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs7162781	0.95[CHB][hapmap];0.89[JPT][hapmap];0.91[ASN][1000 genomes]
rs7167184	0.89[ASN][1000 genomes]
rs7168755	0.90[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs7176721	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7179293	0.85[CHB][hapmap];0.84[JPT][hapmap];0.80[AMR][1000 genomes]
rs7179608	0.91[ASN][1000 genomes]
rs7180675	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72725079	0.89[ASN][1000 genomes]
rs72725080	0.89[ASN][1000 genomes]
rs72725084	0.89[ASN][1000 genomes]
rs72725093	0.91[ASN][1000 genomes]
rs72725101	0.91[ASN][1000 genomes]
rs768663	0.82[EUR][1000 genomes]
rs8026916	0.89[ASN][1000 genomes]
rs8029602	0.95[CHB][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs8032289	0.89[ASN][1000 genomes]
rs8034594	0.85[CHB][hapmap];0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs8036376	0.80[CHB][hapmap]
rs8039035	0.81[JPT][hapmap];0.80[AMR][1000 genomes]
rs884584	0.90[CHB][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs949646	0.80[CHB][hapmap]
rs9806365	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs999393	0.90[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049682	chr15:39657279-40027403	Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv542361	chr15:39657279-40027403	Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	esv3373125	chr15:39691567-40061262	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv904094	chr15:39738006-39976057	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv832977	chr15:39817512-39981520	Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	nsv1048628	chr15:39877498-39940104	Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv832978	chr15:39899759-40094881	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:39923800-39939600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:39934800-39938200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr15:39935200-39938600	Enhancers	Placenta Amnion	Placenta Amnion
4	chr15:39936400-39938200	Enhancers	Right Ventricle	heart
5	chr15:39936400-39938400	Enhancers	Left Ventricle	heart
6	chr15:39937000-39941200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr15:39937400-39938200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr15:39937400-39938200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr15:39937400-39938800	Flanking Active TSS	HepG2	liver
10	chr15:39937600-39938400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr15:39937600-39938400	Enhancers	Esophagus	oesophagus
12	chr15:39937800-39938400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr15:39937800-39943200	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr15:39938000-39944400	Weak transcription	HSMMtube	muscle
15	chr15:39938000-39950000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr15:39938000-39957600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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