Variant report

Variant	rs2013764
Chromosome Location	chr4:79174723-79174724
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10028072	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1017646	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1017647	1.00[ASN][1000 genomes]
rs1017648	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1017650	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1017651	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11098114	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11098131	0.95[ASN][1000 genomes]
rs11941234	1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs13118323	1.00[ASN][1000 genomes]
rs1378237	1.00[ASN][1000 genomes]
rs1378238	1.00[ASN][1000 genomes]
rs1454894	1.00[ASN][1000 genomes]
rs1454895	0.95[ASN][1000 genomes]
rs1454900	1.00[ASN][1000 genomes]
rs1454901	1.00[ASN][1000 genomes]
rs1580105	1.00[ASN][1000 genomes]
rs17003069	0.95[ASN][1000 genomes]
rs17003070	0.95[ASN][1000 genomes]
rs17003071	0.95[ASN][1000 genomes]
rs17003092	1.00[ASN][1000 genomes]
rs17003108	1.00[ASN][1000 genomes]
rs1823921	0.95[ASN][1000 genomes]
rs1840390	1.00[ASN][1000 genomes]
rs1840393	1.00[ASN][1000 genomes]
rs1952400	1.00[ASN][1000 genomes]
rs1999053	1.00[ASN][1000 genomes]
rs2008587	1.00[ASN][1000 genomes]
rs2013770	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2045169	1.00[ASN][1000 genomes]
rs2124145	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2225198	1.00[ASN][1000 genomes]
rs2867014	1.00[ASN][1000 genomes]
rs28803795	0.82[ASN][1000 genomes]
rs28806931	0.82[ASN][1000 genomes]
rs345503	1.00[ASN][1000 genomes]
rs345506	1.00[ASN][1000 genomes]
rs345528	0.82[ASN][1000 genomes]
rs4859919	1.00[ASN][1000 genomes]
rs4859921	1.00[ASN][1000 genomes]
rs4859922	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60544673	0.95[ASN][1000 genomes]
rs60608669	0.82[ASN][1000 genomes]
rs60862246	0.91[ASN][1000 genomes]
rs61283188	1.00[ASN][1000 genomes]
rs6533564	1.00[ASN][1000 genomes]
rs6814182	0.84[ASN][1000 genomes]
rs6820900	1.00[ASN][1000 genomes]
rs6822551	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6822773	0.95[ASN][1000 genomes]
rs6846166	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6847377	1.00[ASN][1000 genomes]
rs6850956	1.00[ASN][1000 genomes]
rs6855457	1.00[ASN][1000 genomes]
rs72862191	0.95[ASN][1000 genomes]
rs72862196	0.95[ASN][1000 genomes]
rs72864511	0.91[ASN][1000 genomes]
rs72864520	1.00[ASN][1000 genomes]
rs72864521	1.00[ASN][1000 genomes]
rs72864564	1.00[ASN][1000 genomes]
rs72864567	1.00[ASN][1000 genomes]
rs72864571	1.00[ASN][1000 genomes]
rs72864577	1.00[ASN][1000 genomes]
rs72864587	1.00[ASN][1000 genomes]
rs72866312	0.82[ASN][1000 genomes]
rs7438056	1.00[ASN][1000 genomes]
rs7667670	1.00[ASN][1000 genomes]
rs967635	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534024	chr4:78785189-79437403	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1009633	chr4:78887573-79652236	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv525530	chr4:79024524-79266563	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv1010782	chr4:79057839-79387207	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv829978	chr4:79144453-79291868	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79144200-79176000	Weak transcription	Psoas Muscle	Psoas
2	chr4:79144600-79179000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:79167800-79176000	Weak transcription	Esophagus	oesophagus
4	chr4:79169200-79186200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr4:79169200-79187400	Weak transcription	HSMMtube	muscle
6	chr4:79169600-79187800	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr4:79169800-79197400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr4:79169800-79213800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr4:79170400-79186000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr4:79170600-79176200	Weak transcription	Fetal Heart	heart
11	chr4:79170800-79176000	Weak transcription	Pancreas	Pancrea
12	chr4:79172400-79175400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
13	chr4:79172400-79175800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:79172600-79175000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr4:79172600-79175000	ZNF genes & repeats	Fetal Intestine Small	intestine
16	chr4:79172600-79175200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr4:79172800-79175400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
18	chr4:79173400-79174800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr4:79173400-79175200	Strong transcription	Fetal Intestine Large	intestine
20	chr4:79173600-79177800	Strong transcription	HepG2	liver
21	chr4:79173800-79174800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
22	chr4:79173800-79175200	Strong transcription	Fetal Kidney	kidney
23	chr4:79173800-79175400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
24	chr4:79173800-79186200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr4:79173800-79187000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr4:79173800-79187400	Weak transcription	Fetal Stomach	stomach
27	chr4:79174000-79175000	Strong transcription	Skeletal Muscle Female	skeletal muscle
28	chr4:79174200-79174800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:79174200-79175000	Genic enhancers	H1 Cell Line	embryonic stem cell
30	chr4:79174200-79178000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr4:79174600-79175000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr4:79174600-79175000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
33	chr4:79174600-79175000	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr4:79174600-79175000	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:79174600-79178400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr4:79174600-79186000	Weak transcription	Fetal Lung	lung
37	chr4:79174600-79197400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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