Variant report

Variant	rs17047372
Chromosome Location	chr4:167130279-167130280
allele	A/T
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:35)

rs_ID	r²[population]
rs1373557	0.88[ASN][1000 genomes]
rs1624224	0.88[ASN][1000 genomes]
rs1675011	0.88[ASN][1000 genomes]
rs17047366	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17047371	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17047374	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs353080	0.88[ASN][1000 genomes]
rs353865	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs366504	0.88[ASN][1000 genomes]
rs388102	0.88[ASN][1000 genomes]
rs404307	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs404636	0.88[ASN][1000 genomes]
rs414867	1.00[JPT][hapmap]
rs415644	0.88[ASN][1000 genomes]
rs421692	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs429253	0.88[ASN][1000 genomes]
rs438082	0.88[ASN][1000 genomes]
rs55730505	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55996420	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56056527	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56342710	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57707469	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57858278	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59053618	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59277412	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61308766	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6856537	0.88[ASN][1000 genomes]
rs72978385	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72978401	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72980306	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72980317	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72980354	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72980355	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7690413	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs833487	0.88[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	nsv821638	chr4:166837633-167262625	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1034421	chr4:166961339-167893289	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv537339	chr4:166961339-167893289	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv881029	chr4:167060016-167284757	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:167124800-167132000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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