Variant report

Variant	rs17498416
Chromosome Location	chr7:113023031-113023032
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10500026	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12705858	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13227231	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13227345	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13230022	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13234348	0.83[ASN][1000 genomes]
rs13240515	0.85[ASN][1000 genomes]
rs13246534	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13246541	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1357744	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1524443	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1701829	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17136276	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17413268	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17413351	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17498088	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2091159	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2396621	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34349491	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34394039	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34448224	0.88[ASN][1000 genomes]
rs34489788	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35080497	0.85[ASN][1000 genomes]
rs35152946	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55924370	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs55957513	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55993020	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56205248	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56258749	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs60321964	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs60454787	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62487666	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62487718	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62487719	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62490164	0.85[ASN][1000 genomes]
rs6943756	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6975850	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6977108	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7780151	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7780773	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7784560	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7786455	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7791408	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7792063	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7796421	0.82[ASN][1000 genomes]
rs7808415	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs881918	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3355135	chr7:112616979-113134651	Active TSS Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv435847	chr7:112618576-113134022	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3430638	chr7:112620663-113134403	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv3442221	chr7:112620665-113134971	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv993501	chr7:112625029-113125338	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv1022066	chr7:112630168-113122748	Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv539090	chr7:112630168-113122748	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv889062	chr7:112920080-113138047	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv831098	chr7:112936711-113090844	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	esv1797684	chr7:113021972-113028663	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17498416	ZNF277	cis	parietal	SCAN

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:113009000-113024200	Weak transcription	Fetal Brain Female	brain
2	chr7:113023000-113024000	Enhancers	Fetal Brain Male	brain

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