Variant report

Variant	rs9285496
Chromosome Location	chr6:142229817-142229818
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:142225504..142227583-chr6:142228227..142231169,2	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1006256	0.87[ASN][1000 genomes]
rs10499228	0.88[ASN][1000 genomes]
rs1125602	0.91[ASN][1000 genomes]
rs12207173	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12664387	0.95[ASN][1000 genomes]
rs13191355	0.97[ASN][1000 genomes]
rs13199965	0.88[ASN][1000 genomes]
rs13203129	0.91[ASN][1000 genomes]
rs13205554	0.91[ASN][1000 genomes]
rs13216616	0.93[ASN][1000 genomes]
rs13219922	0.91[ASN][1000 genomes]
rs1336272	0.93[ASN][1000 genomes]
rs1414743	0.87[ASN][1000 genomes]
rs1537864	0.93[ASN][1000 genomes]
rs17071180	0.91[ASN][1000 genomes]
rs17071231	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2039608	0.91[ASN][1000 genomes]
rs2152589	0.91[ASN][1000 genomes]
rs2784947	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34694977	0.93[ASN][1000 genomes]
rs36042829	0.93[ASN][1000 genomes]
rs4434485	0.88[ASN][1000 genomes]
rs4642496	0.92[ASN][1000 genomes]
rs56086504	0.91[ASN][1000 genomes]
rs56259365	0.93[ASN][1000 genomes]
rs60833819	0.92[ASN][1000 genomes]
rs66470467	0.97[ASN][1000 genomes]
rs67214925	0.93[ASN][1000 genomes]
rs6917831	0.95[ASN][1000 genomes]
rs6917832	0.97[ASN][1000 genomes]
rs6918138	0.97[ASN][1000 genomes]
rs7754052	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7767107	0.88[ASN][1000 genomes]
rs7774022	0.97[ASN][1000 genomes]
rs7775955	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9496171	0.88[ASN][1000 genomes]
rs9496172	0.87[ASN][1000 genomes]
rs9496179	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9496192	0.97[ASN][1000 genomes]
rs9496193	0.97[ASN][1000 genomes]
rs9496196	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015835	chr6:141713451-142233317	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv538455	chr6:141713451-142233317	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1032184	chr6:141909953-142234993	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv830823	chr6:142111420-142305417	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv464066	chr6:142130009-142236578	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv604790	chr6:142130009-142236578	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv886728	chr6:142130009-142245981	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1029504	chr6:142131846-142333198	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv538458	chr6:142131846-142333198	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv1017195	chr6:142142454-142336722	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv886729	chr6:142192725-142277769	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv604792	chr6:142192725-142399251	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
13	nsv464067	chr6:142214093-142283198	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
14	nsv604793	chr6:142214093-142283198	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
15	nsv886730	chr6:142214093-142299345	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142229600-142230000	Active TSS	Liver	Liver
2	chr6:142229800-142230800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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