Variant report

Variant	rs7007342
Chromosome Location	chr8:35590937-35590938
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs1001355	1.00[ASN][1000 genomes]
rs10503982	1.00[ASN][1000 genomes]
rs10954989	1.00[ASN][1000 genomes]
rs11985782	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11988094	1.00[CEU][hapmap];1.00[TSI][hapmap]
rs11995446	1.00[CEU][hapmap]
rs11995471	1.00[CEU][hapmap]
rs12541844	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12543831	0.89[ASN][1000 genomes]
rs12543917	1.00[ASN][1000 genomes]
rs12545460	0.91[ASN][1000 genomes]
rs12547338	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12548530	0.95[ASN][1000 genomes]
rs12548652	1.00[ASN][1000 genomes]
rs12549599	1.00[ASN][1000 genomes]
rs12549774	0.95[ASN][1000 genomes]
rs12550434	1.00[ASN][1000 genomes]
rs12550498	1.00[EUR][1000 genomes]
rs12675805	1.00[EUR][1000 genomes]
rs12678392	1.00[ASN][1000 genomes]
rs12679845	1.00[ASN][1000 genomes]
rs12681078	1.00[ASN][1000 genomes]
rs16875853	0.95[ASN][1000 genomes]
rs16875855	0.95[ASN][1000 genomes]
rs16884235	0.86[ASN][1000 genomes]
rs16884240	0.86[ASN][1000 genomes]
rs16884241	0.89[ASN][1000 genomes]
rs16884255	0.95[ASN][1000 genomes]
rs16884258	0.95[ASN][1000 genomes]
rs16884264	0.95[ASN][1000 genomes]
rs16884266	0.95[ASN][1000 genomes]
rs16884280	1.00[ASN][1000 genomes]
rs16884285	1.00[ASN][1000 genomes]
rs16884301	1.00[CEU][hapmap];1.00[TSI][hapmap]
rs16884351	1.00[ASN][1000 genomes]
rs16884365	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16884373	1.00[ASN][1000 genomes]
rs16884441	1.00[CEU][hapmap];1.00[TSI][hapmap]
rs16884444	1.00[CEU][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap]
rs1992090	0.98[ASN][1000 genomes]
rs2406165	0.89[ASN][1000 genomes]
rs2897334	0.89[ASN][1000 genomes]
rs3802318	0.83[CHD][hapmap];0.81[MEX][hapmap];0.84[ASN][1000 genomes]
rs3824287	1.00[ASN][1000 genomes]
rs4739421	0.88[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs4739422	1.00[ASN][1000 genomes]
rs4739423	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4739424	1.00[ASN][1000 genomes]
rs61357978	1.00[ASN][1000 genomes]
rs6983275	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6987079	1.00[CEU][hapmap];1.00[TSI][hapmap]
rs6996645	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6998947	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73583045	0.89[ASN][1000 genomes]
rs73583047	0.89[ASN][1000 genomes]
rs73583049	0.95[ASN][1000 genomes]
rs73584844	1.00[ASN][1000 genomes]
rs73584850	1.00[ASN][1000 genomes]
rs73586708	1.00[ASN][1000 genomes]
rs7812475	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7818904	1.00[ASN][1000 genomes]
rs7820516	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7824105	1.00[CEU][hapmap]
rs7824631	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7844971	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7846338	1.00[ASN][1000 genomes]
rs934649	1.00[CEU][hapmap];1.00[TSI][hapmap]
rs966868	0.95[ASN][1000 genomes]
rs966869	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017085	chr8:34742896-35594241	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv539546	chr8:34742896-35594241	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv533420	chr8:35358115-36227536	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv831285	chr8:35485874-35648117	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv2754662	chr8:35558658-35648958	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv1032540	chr8:35565491-35949132	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:35575000-35600200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:35576000-35631600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr8:35582000-35640600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr8:35584400-35598000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr8:35584600-35603200	Weak transcription	Fetal Brain Female	brain
6	chr8:35587200-35594400	Weak transcription	Small Intestine	intestine
7	chr8:35588000-35598000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr8:35589600-35603400	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr8:35589800-35591000	Enhancers	Fetal Kidney	kidney
10	chr8:35590000-35591600	Strong transcription	H1 Cell Line	embryonic stem cell
11	chr8:35590000-35591800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr8:35590000-35591800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:35590200-35591200	Enhancers	Fetal Intestine Large	intestine
14	chr8:35590200-35591400	Enhancers	Fetal Intestine Small	intestine
15	chr8:35590200-35591400	Enhancers	Stomach Mucosa	stomach
16	chr8:35590200-35597200	Weak transcription	Fetal Brain Male	brain
17	chr8:35590200-35606000	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr8:35590400-35591400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr8:35590400-35591800	Strong transcription	H9 Cell Line	embryonic stem cell
20	chr8:35590400-35591800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:35590600-35591400	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr8:35590800-35591200	Strong transcription	HUES48 Cell Line	embryonic stem cell
23	chr8:35590800-35591200	Enhancers	Duodenum Mucosa	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links