Variant report

Variant	rs73586708
Chromosome Location	chr8:35594386-35594387
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs1001355	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10503982	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10954989	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11985782	0.86[ASN][1000 genomes]
rs12541844	1.00[ASN][1000 genomes]
rs12543831	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12543917	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12545460	0.91[ASN][1000 genomes]
rs12546354	0.86[EUR][1000 genomes]
rs12547338	1.00[ASN][1000 genomes]
rs12548530	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12548652	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12549599	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12549774	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12550434	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12678392	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12679845	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12681078	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16875853	0.95[ASN][1000 genomes]
rs16875855	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16884235	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16884240	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16884241	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16884255	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16884258	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16884264	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16884266	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16884280	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16884285	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16884351	0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16884365	1.00[ASN][1000 genomes]
rs16884373	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1992090	0.98[ASN][1000 genomes]
rs2406165	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2897334	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3802318	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3824287	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4739421	0.86[ASN][1000 genomes]
rs4739422	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4739423	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4739424	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61357978	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6983275	1.00[ASN][1000 genomes]
rs6996645	1.00[ASN][1000 genomes]
rs6998947	1.00[ASN][1000 genomes]
rs7007342	1.00[ASN][1000 genomes]
rs73583045	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73583047	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73583049	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73584844	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73584850	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7812475	1.00[ASN][1000 genomes]
rs7818904	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7820516	1.00[ASN][1000 genomes]
rs7824631	1.00[ASN][1000 genomes]
rs7844971	0.98[ASN][1000 genomes]
rs7846338	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs966868	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs966869	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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:22 , 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	chr8:35590200-35597200	Weak transcription	Fetal Brain Male	brain
10	chr8:35590200-35606000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr8:35591200-35594600	Weak transcription	Fetal Intestine Large	intestine
12	chr8:35591200-35598000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr8:35591400-35608000	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr8:35591600-35611800	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr8:35591800-35608000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:35591800-35611200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr8:35591800-35611800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr8:35594000-35596400	Enhancers	Fetal Lung	lung
19	chr8:35594200-35594400	Enhancers	Duodenum Mucosa	Duodenum
20	chr8:35594200-35595200	Enhancers	Fetal Heart	heart
21	chr8:35594200-35595200	Enhancers	Fetal Kidney	kidney
22	chr8:35594200-35595400	Enhancers	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links