Variant report

Variant	rs847269
Chromosome Location	chr14:72705328-72705329
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs2158986	0.95[CHB][hapmap];0.94[JPT][hapmap];0.85[YRI][hapmap];0.89[ASN][1000 genomes]
rs2158988	0.91[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs2238241	0.91[CHB][hapmap]
rs2238242	0.91[CHB][hapmap]
rs2529646	0.95[ASN][1000 genomes]
rs2529647	0.95[ASN][1000 genomes]
rs4902998	0.81[CHB][hapmap]
rs57141704	0.83[ASN][1000 genomes]
rs58600935	0.87[ASN][1000 genomes]
rs6574054	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.92[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs699360	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs699361	0.94[CHB][hapmap];0.94[JPT][hapmap];0.94[YRI][hapmap];0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs699362	0.90[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs699368	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8022525	0.95[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs8022968	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs847235	0.83[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs847236	0.83[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs847239	0.83[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs847240	0.83[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs847254	0.86[CHB][hapmap];0.94[JPT][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs847259	0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs847262	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs847263	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs847264	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs847265	0.91[CHB][hapmap];0.94[JPT][hapmap];0.84[YRI][hapmap];0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs847266	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs847267	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs847268	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs847270	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs847271	1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[YRI][hapmap];0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs847272	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs847273	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap]
rs847274	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs847275	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs847276	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs847277	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs847278	0.94[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs847279	0.94[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs847297	0.86[CHB][hapmap]
rs847302	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.92[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs847305	0.90[CHB][hapmap];0.87[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs847307	0.95[CHB][hapmap];0.94[JPT][hapmap];0.90[YRI][hapmap];0.87[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs847308	0.95[CHB][hapmap];0.94[JPT][hapmap];0.96[ASN][1000 genomes]
rs847310	1.00[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs847313	0.90[ASN][1000 genomes]
rs847314	0.83[JPT][hapmap];0.82[ASN][1000 genomes]
rs847318	0.86[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs847319	0.86[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs847320	0.86[ASN][1000 genomes]
rs847321	0.91[CHB][hapmap];0.89[JPT][hapmap];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv948800	chr14:72462557-73150701	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1041492	chr14:72634606-72768970	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72687800-72705800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr14:72699800-72719600	Weak transcription	Right Ventricle	heart
3	chr14:72700600-72709800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr14:72703400-72706600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr14:72704000-72706800	Enhancers	Primary B cells from peripheral blood	blood
6	chr14:72705200-72706800	Enhancers	Primary hematopoietic stem cells	blood
7	chr14:72705200-72707000	Enhancers	Fetal Thymus	thymus

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