Variant report

Variant	rs10815856
Chromosome Location	chr9:8408582-8408583
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10116650	1.00[JPT][hapmap]
rs10123746	1.00[JPT][hapmap]
rs1021720	1.00[JPT][hapmap]
rs10511494	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10815845	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10815846	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10815847	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10815849	0.97[ASN][1000 genomes]
rs10815855	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10815857	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.94[ASN][1000 genomes]
rs10977024	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.94[ASN][1000 genomes]
rs10977035	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10977046	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.94[ASN][1000 genomes]
rs10977052	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10977057	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10977059	1.00[CHB][hapmap];0.82[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10977062	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10977064	0.97[ASN][1000 genomes]
rs10977073	0.97[ASN][1000 genomes]
rs10977074	0.97[ASN][1000 genomes]
rs10977084	1.00[YRI][hapmap]
rs10977089	1.00[YRI][hapmap]
rs10977092	1.00[JPT][hapmap]
rs10977093	1.00[JPT][hapmap]
rs12376680	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs12377175	0.84[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs12685058	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.91[ASN][1000 genomes]
rs12686400	1.00[CHB][hapmap]
rs1500331	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17561379	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1909755	1.00[YRI][hapmap]
rs1909757	1.00[JPT][hapmap]
rs1909758	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2381797	1.00[JPT][hapmap]

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	nsv8414	chr9:7827373-8511613	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1031472	chr9:8250901-8712547	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv1022796	chr9:8360729-9110046	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv973439	chr9:8406003-8408876	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
5	nsv613287	chr9:8408453-8422302	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8389600-8451000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr9:8394000-8424400	Weak transcription	Fetal Lung	lung
3	chr9:8396000-8410400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:8402400-8408600	Weak transcription	Brain Germinal Matrix	brain
5	chr9:8402400-8421000	Weak transcription	Brain Hippocampus Middle	brain
6	chr9:8402600-8408600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:8402600-8448800	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr9:8402800-8438000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr9:8405800-8438000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr9:8407600-8410800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr9:8407600-8410800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr9:8407800-8410600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr9:8407800-8414600	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr9:8408000-8408800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr9:8408000-8408800	Enhancers	Brain Anterior Caudate	brain
16	chr9:8408000-8410600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr9:8408200-8408800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr9:8408200-8409400	Weak transcription	Brain Angular Gyrus	brain
19	chr9:8408200-8409800	Weak transcription	Brain Substantia Nigra	brain
20	chr9:8408200-8429200	Weak transcription	Brain Cingulate Gyrus	brain
21	chr9:8408400-8408600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr9:8408400-8408800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr9:8408400-8409200	Enhancers	Dnd41	blood
24	chr9:8408400-8410400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr9:8408400-8410600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links