Variant report

Variant	rs7775955
Chromosome Location	chr6:142209706-142209707
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1006256	0.81[ASN][1000 genomes]
rs10499228	0.94[ASN][1000 genomes]
rs1125602	0.98[ASN][1000 genomes]
rs12207173	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12664387	0.89[ASN][1000 genomes]
rs13191355	0.90[ASN][1000 genomes]
rs13199965	0.94[ASN][1000 genomes]
rs13203129	0.98[ASN][1000 genomes]
rs13205554	0.98[ASN][1000 genomes]
rs13216616	0.86[ASN][1000 genomes]
rs13219922	0.98[ASN][1000 genomes]
rs1336272	0.87[ASN][1000 genomes]
rs1414743	0.81[ASN][1000 genomes]
rs1537864	0.86[ASN][1000 genomes]
rs17071180	0.98[ASN][1000 genomes]
rs17071231	0.90[ASN][1000 genomes]
rs2039608	0.98[ASN][1000 genomes]
rs2152589	0.98[ASN][1000 genomes]
rs2784947	0.82[ASN][1000 genomes]
rs34694977	0.96[ASN][1000 genomes]
rs36042829	0.86[ASN][1000 genomes]
rs4434485	0.83[ASN][1000 genomes]
rs4642496	0.86[ASN][1000 genomes]
rs56086504	0.98[ASN][1000 genomes]
rs56259365	0.96[ASN][1000 genomes]
rs60833819	0.86[ASN][1000 genomes]
rs66470467	0.91[ASN][1000 genomes]
rs67214925	0.86[ASN][1000 genomes]
rs6917831	0.89[ASN][1000 genomes]
rs6917832	0.90[ASN][1000 genomes]
rs6918138	0.90[ASN][1000 genomes]
rs7754052	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7767107	0.94[ASN][1000 genomes]
rs7774022	0.90[ASN][1000 genomes]
rs9285496	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9496171	0.94[ASN][1000 genomes]
rs9496172	0.93[ASN][1000 genomes]
rs9496179	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9496192	0.90[ASN][1000 genomes]
rs9496193	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 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	nsv604791	chr6:142174962-142214093	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
12	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
13	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

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142207800-142211400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:142209000-142211400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:142209000-142212000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:142209000-142215000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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