Variant report

Variant	rs9363305
Chromosome Location	chr6:65698357-65698358
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:65695796..65698770-chr6:65700016..65702026,2	K562	blood:

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs11752311	0.83[ASN][1000 genomes]
rs11756218	0.87[ASN][1000 genomes]
rs11757845	0.87[ASN][1000 genomes]
rs11758096	0.83[ASN][1000 genomes]
rs11759933	0.84[ASN][1000 genomes]
rs12175848	0.84[ASN][1000 genomes]
rs17688615	0.90[ASN][1000 genomes]
rs2024834	0.83[ASN][1000 genomes]
rs2224207	0.83[ASN][1000 genomes]
rs2349998	0.95[ASN][1000 genomes]
rs2349999	0.90[ASN][1000 genomes]
rs28493571	0.86[ASN][1000 genomes]
rs28546411	0.87[ASN][1000 genomes]
rs28583858	0.83[ASN][1000 genomes]
rs34346075	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4710290	0.83[EUR][1000 genomes]
rs718017	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs72875929	0.90[ASN][1000 genomes]
rs72875932	0.90[ASN][1000 genomes]
rs72875936	0.90[ASN][1000 genomes]
rs72875953	0.90[ASN][1000 genomes]
rs72875955	0.90[ASN][1000 genomes]
rs72875958	0.90[ASN][1000 genomes]
rs72875962	0.90[ASN][1000 genomes]
rs72875963	0.90[ASN][1000 genomes]
rs72875965	0.90[ASN][1000 genomes]
rs72875967	0.90[ASN][1000 genomes]
rs72875968	0.90[ASN][1000 genomes]
rs72875972	0.87[ASN][1000 genomes]
rs72875975	0.87[ASN][1000 genomes]
rs72875977	0.84[ASN][1000 genomes]
rs72875979	0.87[ASN][1000 genomes]
rs7738129	0.85[ASN][1000 genomes]
rs7760665	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7765697	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9342454	0.90[ASN][1000 genomes]
rs9345571	0.83[ASN][1000 genomes]
rs9345573	0.84[ASN][1000 genomes]
rs9345574	0.87[ASN][1000 genomes]
rs9345575	0.90[ASN][1000 genomes]
rs9345576	0.90[ASN][1000 genomes]
rs9345578	0.90[ASN][1000 genomes]
rs9345582	0.86[ASN][1000 genomes]
rs9345583	0.86[ASN][1000 genomes]
rs9345584	0.86[ASN][1000 genomes]
rs9345585	0.84[ASN][1000 genomes]
rs9345591	0.85[ASN][1000 genomes]
rs9351475	0.90[ASN][1000 genomes]
rs9351477	0.90[ASN][1000 genomes]
rs9354194	0.84[ASN][1000 genomes]
rs9354195	0.84[ASN][1000 genomes]
rs9354196	0.90[ASN][1000 genomes]
rs9354197	0.90[ASN][1000 genomes]
rs9354199	0.86[ASN][1000 genomes]
rs9354203	0.84[ASN][1000 genomes]
rs9360100	0.83[ASN][1000 genomes]
rs9360103	0.90[ASN][1000 genomes]
rs9360105	0.86[ASN][1000 genomes]
rs9360106	0.86[ASN][1000 genomes]
rs9360109	0.84[ASN][1000 genomes]
rs9363299	0.83[ASN][1000 genomes]
rs9363301	0.83[CHB][hapmap];0.85[JPT][hapmap];0.90[ASN][1000 genomes]
rs9363302	0.90[ASN][1000 genomes]
rs9363303	0.90[ASN][1000 genomes]
rs9363304	0.90[ASN][1000 genomes]
rs9363307	0.90[ASN][1000 genomes]
rs9363308	0.90[ASN][1000 genomes]
rs9363309	0.87[ASN][1000 genomes]
rs9363310	0.86[ASN][1000 genomes]
rs9363311	0.86[ASN][1000 genomes]
rs9363312	0.86[ASN][1000 genomes]
rs9363313	0.86[ASN][1000 genomes]
rs9363314	0.84[ASN][1000 genomes]
rs9453127	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1020411	chr6:65321029-65854790	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv538276	chr6:65321029-65854790	ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1024611	chr6:65379523-65736399	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1034253	chr6:65390865-65865124	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv538278	chr6:65390865-65865124	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv949287	chr6:65422320-65828488	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv533301	chr6:65435076-65704216	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv948458	chr6:65463110-65828488	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
9	nsv1033186	chr6:65493291-65700532	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv933558	chr6:65524861-65760189	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
11	nsv603406	chr6:65571770-65712288	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv1034043	chr6:65573463-65823028	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
13	nsv1034230	chr6:65579061-65887750	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
14	nsv933464	chr6:65596504-65767718	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
15	nsv933937	chr6:65596504-65926900	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
16	nsv933776	chr6:65598694-65760189	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
17	nsv1022556	chr6:65624150-65914258	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
18	nsv934051	chr6:65625209-65926900	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
19	nsv603407	chr6:65637508-65709059	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
20	nsv1025681	chr6:65640647-65700532	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
21	nsv886008	chr6:65650698-65722525	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
22	nsv934217	chr6:65655722-65767718	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
23	nsv933140	chr6:65655722-65814323	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:65697000-65698600	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr6:65697600-65699000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:65697600-65700000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:65698000-65698400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr6:65698200-65698800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr6:65698200-65699200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr6:65698200-65705000	Weak transcription	Pancreas	Pancrea

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