Variant report

Variant	rs9447795
Chromosome Location	chr6:77471306-77471307
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1017707	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1017708	0.97[EUR][1000 genomes]
rs12200640	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12208150	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12528989	0.83[AMR][1000 genomes]
rs13207756	0.81[AMR][1000 genomes]
rs1379667	0.97[EUR][1000 genomes]
rs1381675	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1457948	0.97[EUR][1000 genomes]
rs1457949	0.97[EUR][1000 genomes]
rs1457950	0.95[EUR][1000 genomes]
rs1457952	0.97[EUR][1000 genomes]
rs1457962	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1545651	0.83[AMR][1000 genomes]
rs1598867	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1809246	0.83[AMR][1000 genomes]
rs2061648	0.97[EUR][1000 genomes]
rs2125215	0.96[EUR][1000 genomes]
rs2199007	0.83[AMR][1000 genomes]
rs35840118	0.81[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs4264999	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4708284	0.97[EUR][1000 genomes]
rs6453936	0.96[EUR][1000 genomes]
rs6900429	0.97[EUR][1000 genomes]
rs6901108	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6925529	0.97[EUR][1000 genomes]
rs6938021	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7739924	0.97[EUR][1000 genomes]
rs7740357	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7744044	0.97[EUR][1000 genomes]
rs9352378	0.86[AMR][1000 genomes]
rs9359219	0.83[AMR][1000 genomes]
rs9447796	0.97[EUR][1000 genomes]
rs9447797	0.97[EUR][1000 genomes]
rs969251	0.97[EUR][1000 genomes]
rs987007	0.97[EUR][1000 genomes]
rs987008	0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025439	chr6:77093795-77479689	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv538320	chr6:77093795-77479689	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1026054	chr6:77294100-77479689	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1019520	chr6:77355212-77875164	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv538321	chr6:77355212-77875164	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv886217	chr6:77415155-77490717	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv886218	chr6:77415155-77500526	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv886220	chr6:77415155-77505717	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv886219	chr6:77415155-77515516	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	esv2757180	chr6:77418087-77476663	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv2759444	chr6:77418087-77476663	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3391366	chr6:77452282-77476828	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
13	esv3415838	chr6:77452282-77485905	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	esv3448552	chr6:77461282-77485905	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:77470600-77484600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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