Variant report

Variant	rs652867
Chromosome Location	chr9:97307701-97307702
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10115929	0.86[ASN][1000 genomes]
rs10119419	0.86[ASN][1000 genomes]
rs10733753	0.86[ASN][1000 genomes]
rs10761331	0.86[ASN][1000 genomes]
rs10761332	0.86[ASN][1000 genomes]
rs10761333	0.86[ASN][1000 genomes]
rs10821364	0.85[ASN][1000 genomes]
rs10821365	0.86[ASN][1000 genomes]
rs10821367	0.86[ASN][1000 genomes]
rs10821369	0.83[ASN][1000 genomes]
rs10993226	0.80[AMR][1000 genomes]
rs10993241	0.87[ASN][1000 genomes]
rs10993242	0.86[ASN][1000 genomes]
rs11790263	0.86[ASN][1000 genomes]
rs12552009	0.84[AMR][1000 genomes]
rs2280300	0.86[ASN][1000 genomes]
rs2460138	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs2679599	0.84[AFR][1000 genomes]
rs2679600	0.84[AFR][1000 genomes]
rs2679602	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2679611	0.84[AMR][1000 genomes]
rs2772013	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2772022	0.84[AFR][1000 genomes]
rs2790390	0.84[AFR][1000 genomes]
rs2790400	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2790404	0.83[AMR][1000 genomes]
rs2945802	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2987882	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs2987888	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2987889	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2993975	0.83[AMR][1000 genomes]
rs3864788	0.86[ASN][1000 genomes]
rs4744353	0.86[ASN][1000 genomes]
rs479197	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs488270	0.82[ASN][1000 genomes]
rs514222	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs515339	0.92[AFR][1000 genomes]
rs518768	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs540124	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs543698	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs543731	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs547693	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs549615	0.84[AMR][1000 genomes]
rs572689	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs573371	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs573847	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs583365	0.84[AFR][1000 genomes]
rs590090	0.84[AFR][1000 genomes]
rs605323	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs606207	0.85[AMR][1000 genomes]
rs607160	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs608837	0.84[AMR][1000 genomes]
rs632506	0.92[AFR][1000 genomes]
rs678363	0.80[EUR][1000 genomes]
rs688843	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs693399	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7048277	0.86[ASN][1000 genomes]
rs781650	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7867912	0.85[ASN][1000 genomes]
rs802918	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs802919	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs874248	0.84[AFR][1000 genomes]
rs9409801	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs965474	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761545	chr9:97025298-97356950	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1041195	chr9:97054795-97402378	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	esv1840205	chr9:97202200-97366400	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv893595	chr9:97268182-97330693	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv525298	chr9:97289583-97312584	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97296400-97314200	Weak transcription	Liver	Liver
2	chr9:97297200-97315000	Weak transcription	HepG2	liver
3	chr9:97302600-97315000	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr9:97304600-97307800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr9:97304800-97315200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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