Variant report

Variant	rs9462122
Chromosome Location	chr6:35778326-35778327
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 113 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:102)

rs_ID	r²[population]
rs10484264	0.95[ASN][1000 genomes]
rs1049649	0.95[ASN][1000 genomes]
rs10947572	0.93[ASN][1000 genomes]
rs10947574	0.92[ASN][1000 genomes]
rs10947576	0.84[ASN][1000 genomes]
rs11964319	0.96[ASN][1000 genomes]
rs11968149	0.95[ASN][1000 genomes]
rs12526050	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1326752	0.92[ASN][1000 genomes]
rs1326756	0.91[ASN][1000 genomes]
rs17653835	0.95[ASN][1000 genomes]
rs17654270	0.92[ASN][1000 genomes]
rs17705020	0.95[ASN][1000 genomes]
rs1887170	0.92[ASN][1000 genomes]
rs2038962	0.95[ASN][1000 genomes]
rs2182546	0.89[ASN][1000 genomes]
rs2250151	0.84[ASN][1000 genomes]
rs2301510	0.84[ASN][1000 genomes]
rs2395638	0.95[ASN][1000 genomes]
rs2395641	0.87[ASN][1000 genomes]
rs2395644	0.83[ASN][1000 genomes]
rs2395646	0.82[ASN][1000 genomes]
rs2766519	0.81[ASN][1000 genomes]
rs2766520	0.82[ASN][1000 genomes]
rs2766521	0.82[ASN][1000 genomes]
rs2766525	0.97[ASN][1000 genomes]
rs2817022	0.82[ASN][1000 genomes]
rs2817023	0.86[ASN][1000 genomes]
rs2817027	0.80[ASN][1000 genomes]
rs3891863	0.92[ASN][1000 genomes]
rs3997732	0.87[ASN][1000 genomes]
rs4340986	0.95[ASN][1000 genomes]
rs60467728	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60696013	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6457857	0.97[ASN][1000 genomes]
rs6457858	0.95[ASN][1000 genomes]
rs6457859	0.95[ASN][1000 genomes]
rs6457862	0.95[ASN][1000 genomes]
rs6457864	0.92[ASN][1000 genomes]
rs6905144	0.95[ASN][1000 genomes]
rs6906455	0.91[ASN][1000 genomes]
rs6908433	0.82[ASN][1000 genomes]
rs6910260	0.80[ASN][1000 genomes]
rs6910906	0.95[ASN][1000 genomes]
rs6911849	0.92[ASN][1000 genomes]
rs6916941	0.92[ASN][1000 genomes]
rs6922695	0.95[ASN][1000 genomes]
rs6926156	0.92[ASN][1000 genomes]
rs6931888	0.95[ASN][1000 genomes]
rs6932973	0.95[ASN][1000 genomes]
rs6933287	0.95[ASN][1000 genomes]
rs721694	0.93[ASN][1000 genomes]
rs7740886	0.95[ASN][1000 genomes]
rs7744924	0.92[ASN][1000 genomes]
rs7749862	0.92[ASN][1000 genomes]
rs7752551	0.95[ASN][1000 genomes]
rs7755600	0.84[ASN][1000 genomes]
rs7758042	0.95[ASN][1000 genomes]
rs7763752	0.82[ASN][1000 genomes]
rs7774060	0.95[ASN][1000 genomes]
rs7776342	0.95[ASN][1000 genomes]
rs880062	0.97[ASN][1000 genomes]
rs9296166	0.95[ASN][1000 genomes]
rs9462125	0.95[ASN][1000 genomes]
rs9462128	0.95[ASN][1000 genomes]
rs9462131	0.95[ASN][1000 genomes]
rs9462132	0.95[ASN][1000 genomes]
rs9462134	0.95[ASN][1000 genomes]
rs9462136	0.95[ASN][1000 genomes]
rs9462141	0.92[ASN][1000 genomes]
rs9462143	0.83[ASN][1000 genomes]
rs9462144	0.81[ASN][1000 genomes]
rs9470111	0.95[ASN][1000 genomes]
rs9470118	0.95[ASN][1000 genomes]
rs9470119	0.89[ASN][1000 genomes]
rs9470120	0.95[ASN][1000 genomes]
rs9470121	0.95[ASN][1000 genomes]
rs9470122	0.95[ASN][1000 genomes]
rs9470124	0.92[ASN][1000 genomes]
rs9470125	0.95[ASN][1000 genomes]
rs9470126	0.95[ASN][1000 genomes]
rs9470130	0.95[ASN][1000 genomes]
rs9470131	0.95[ASN][1000 genomes]
rs9470136	0.95[ASN][1000 genomes]
rs9470138	0.95[ASN][1000 genomes]
rs9470139	0.95[ASN][1000 genomes]
rs9470140	0.92[ASN][1000 genomes]
rs9470141	0.92[ASN][1000 genomes]
rs9470142	0.92[ASN][1000 genomes]
rs9470144	0.92[ASN][1000 genomes]
rs9470151	0.92[ASN][1000 genomes]
rs9470152	0.91[ASN][1000 genomes]
rs9470153	0.92[ASN][1000 genomes]
rs9470154	0.92[ASN][1000 genomes]
rs9470155	0.84[ASN][1000 genomes]
rs9470156	0.84[ASN][1000 genomes]
rs9470157	0.84[ASN][1000 genomes]
rs9470161	0.84[ASN][1000 genomes]
rs9470162	0.84[ASN][1000 genomes]
rs9470166	0.82[ASN][1000 genomes]
rs9470167	0.82[ASN][1000 genomes]
rs9470169	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758048	chr6:35463741-35806504	Genic enhancers Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	esv2759420	chr6:35463741-35806504	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	esv3430300	chr6:35549151-35959004	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	nsv821646	chr6:35604428-35802594	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv885802	chr6:35621781-35787417	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
6	nsv885803	chr6:35621781-35805133	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
7	nsv885804	chr6:35621781-35809776	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
8	nsv428143	chr6:35637083-35806504	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
9	nsv885805	chr6:35685955-35779879	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
10	esv1791730	chr6:35754783-35805144	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
11	nsv602939	chr6:35758072-35783497	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35773000-35791400	Weak transcription	Right Atrium	heart
2	chr6:35773400-35778800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:35773800-35778800	Weak transcription	Pancreas	Pancrea
4	chr6:35776200-35785000	Weak transcription	Brain Anterior Caudate	brain
5	chr6:35776400-35778600	Enhancers	Hela-S3	cervix
6	chr6:35777000-35778800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:35777000-35778800	Weak transcription	Esophagus	oesophagus
8	chr6:35777000-35782400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:35777000-35801400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr6:35777800-35779800	Enhancers	Primary neutrophils fromperipheralblood	blood

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