Variant report

Variant	rs67137307
Chromosome Location	chr4:130999684-130999685
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10518560	1.00[EUR][1000 genomes]
rs1395976	0.88[EUR][1000 genomes]
rs28428490	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28581332	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4864324	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55907609	1.00[EUR][1000 genomes]
rs56932934	1.00[ASN][1000 genomes]
rs61464540	0.89[EUR][1000 genomes]
rs66516628	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66528219	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66920142	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67312336	0.89[EUR][1000 genomes]
rs67499622	0.88[EUR][1000 genomes]
rs67696760	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67814075	0.89[EUR][1000 genomes]
rs67868780	0.88[EUR][1000 genomes]
rs67992570	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs68036106	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs68081878	0.89[EUR][1000 genomes]
rs72678114	0.88[EUR][1000 genomes]
rs72678118	1.00[EUR][1000 genomes]
rs72678137	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72678144	1.00[EUR][1000 genomes]
rs72678151	0.87[EUR][1000 genomes]
rs72678166	0.88[ASN][1000 genomes]
rs72926834	0.88[ASN][1000 genomes]
rs72926848	0.88[ASN][1000 genomes]
rs72926888	1.00[ASN][1000 genomes]
rs72926894	1.00[ASN][1000 genomes]
rs72928857	1.00[ASN][1000 genomes]
rs7670930	0.94[EUR][1000 genomes]
rs7681876	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv595412	chr4:130962263-131001046	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv461640	chr4:130962263-131003605	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv595413	chr4:130962263-131003605	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv1027281	chr4:130962945-131005768	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv1027051	chr4:130962945-131010834	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv1019114	chr4:130962945-131013140	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv1028045	chr4:130965914-131004697	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv595414	chr4:130983055-131024471	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv595415	chr4:130983605-131046911	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv595416	chr4:130998472-131834405	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr4:130995600-131002200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:130995600-131005000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr4:130995800-131001600	Weak transcription	Fetal Intestine Large	intestine
4	chr4:130996000-131001400	Weak transcription	Fetal Intestine Small	intestine
5	chr4:130996000-131001600	Weak transcription	Duodenum Mucosa	Duodenum
6	chr4:130996000-131001600	Weak transcription	Stomach Mucosa	stomach
7	chr4:130996200-131001600	Weak transcription	Liver	Liver
8	chr4:130998200-130999800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:130998200-130999800	Enhancers	HMEC	breast
10	chr4:130998200-131000000	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr4:130999000-130999800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr4:130999200-131002000	Weak transcription	NHEK	skin
13	chr4:130999400-130999800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:130999400-130999800	Enhancers	Placenta Amnion	Placenta Amnion

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links