Variant report

Variant	rs917221
Chromosome Location	chr7:16541388-16541389
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11980729	0.98[ASN][1000 genomes]
rs12535460	0.88[CHB][hapmap];0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs1476092	0.86[EUR][1000 genomes]
rs1990128	0.83[EUR][1000 genomes]
rs1990129	0.83[EUR][1000 genomes]
rs2057959	0.83[EUR][1000 genomes]
rs2108135	0.82[EUR][1000 genomes]
rs2158792	0.82[EUR][1000 genomes]
rs2158793	0.83[EUR][1000 genomes]
rs2158795	0.82[EUR][1000 genomes]
rs2704670	0.89[JPT][hapmap]
rs2704672	0.84[JPT][hapmap]
rs58125563	0.81[ASN][1000 genomes]
rs6461261	0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6461262	0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6952900	0.84[JPT][hapmap]
rs73074756	0.81[ASN][1000 genomes]
rs73074757	0.81[ASN][1000 genomes]
rs73074772	0.81[ASN][1000 genomes]
rs73076713	0.98[ASN][1000 genomes]
rs73076726	0.99[ASN][1000 genomes]
rs73076729	0.90[ASN][1000 genomes]
rs7792141	0.83[EUR][1000 genomes]
rs7801569	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs917222	0.92[EUR][1000 genomes];0.81[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	nsv1016642	chr7:15884061-16799788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv1034151	chr7:16415497-16578081	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
3	nsv887754	chr7:16509086-16541388	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv887755	chr7:16509086-16542364	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv887756	chr7:16520193-16566391	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
6	nsv1028125	chr7:16529160-16847225	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised 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	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16535200-16541600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:16539200-16543000	Weak transcription	Stomach Mucosa	stomach
3	chr7:16541200-16542000	ZNF genes & repeats	Fetal Intestine Small	intestine

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