Variant report

Variant	rs17345417
Chromosome Location	chr4:95948486-95948487
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11097447	1.00[ASW][hapmap]
rs1154847	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs11939949	1.00[ASW][hapmap]
rs12508840	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs13108149	1.00[ASW][hapmap]
rs13134042	1.00[YRI][hapmap]
rs13134763	1.00[YRI][hapmap]
rs1373647	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1596670	1.00[CHB][hapmap]
rs17022863	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17022883	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17022885	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs17343504	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.88[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17415748	1.00[ASW][hapmap]
rs1822827	1.00[ASN][1000 genomes]
rs1836266	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2120833	1.00[ASN][1000 genomes]
rs36024977	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4299590	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs4586955	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs58528248	1.00[ASN][1000 genomes]
rs61018424	1.00[ASN][1000 genomes]
rs6532522	1.00[ASN][1000 genomes]
rs6850046	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs71601251	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71601253	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71601254	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71617619	1.00[ASN][1000 genomes]
rs7681859	1.00[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	nsv932216	chr4:95501261-96109807	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1003860	chr4:95507683-96120619	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv869528	chr4:95537649-96368018	Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv492312	chr4:95823124-96128327	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
5	nsv879622	chr4:95917980-95984379	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv830011	chr4:95947560-96103934	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95941400-95949000	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr4:95947800-95949800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:95948000-95949600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr4:95948000-95949800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:95948000-95949800	Enhancers	A549	lung
6	chr4:95948200-95949200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr4:95948200-95966600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:95948400-95949600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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