Variant report

Variant	rs17011328
Chromosome Location	chr10:49441449-49441450
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:49433973..49437325-chr10:49440787..49445569,4	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11101265	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[EUR][1000 genomes]
rs11101314	1.00[MEX][hapmap]
rs11816450	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11819269	0.84[LWK][hapmap];1.00[MEX][hapmap]
rs12249536	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[EUR][1000 genomes]
rs12252237	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[EUR][1000 genomes]
rs1429801	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[EUR][1000 genomes]
rs1429802	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs1550774	1.00[CEU][hapmap];1.00[GIH][hapmap]
rs1623017	1.00[CEU][hapmap]
rs1881739	1.00[GIH][hapmap]
rs2590379	1.00[CEU][hapmap]
rs2590387	1.00[CEU][hapmap]
rs2590388	1.00[CEU][hapmap]
rs2698769	1.00[GIH][hapmap]
rs280612	1.00[MEX][hapmap]
rs3730154	1.00[CEU][hapmap];1.00[GIH][hapmap]
rs57345918	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58787956	0.86[EUR][1000 genomes]
rs7071514	1.00[MEX][hapmap]
rs7098618	1.00[CEU][hapmap]
rs73294242	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74130209	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7915014	1.00[CEU][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831864	chr10:49299274-49450299	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv895366	chr10:49299274-49576454	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv895367	chr10:49333754-49491047	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv895368	chr10:49381635-49551560	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv467190	chr10:49402084-49576878	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv550811	chr10:49402084-49576878	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv895370	chr10:49421173-49484698	Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49437800-49442000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr10:49440800-49441600	Enhancers	Brain Inferior Temporal Lobe	brain
3	chr10:49441000-49442200	Enhancers	Brain Substantia Nigra	brain
4	chr10:49441000-49444200	Weak transcription	Fetal Thymus	thymus
5	chr10:49441200-49441600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr10:49441200-49442000	Enhancers	Brain Angular Gyrus	brain
7	chr10:49441200-49442600	Enhancers	Right Ventricle	heart
8	chr10:49441400-49441600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr10:49441400-49441600	Enhancers	Brain Anterior Caudate	brain
10	chr10:49441400-49442000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr10:49441400-49443400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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