Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11155422	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12110970	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17797768	0.82[ASN][1000 genomes]
rs17797774	0.82[ASN][1000 genomes]
rs28800626	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6570686	1.00[ASN][1000 genomes]
rs6570687	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6570688	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6570690	0.85[AMR][1000 genomes]
rs6905046	1.00[ASN][1000 genomes]
rs6907972	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6908027	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6910793	1.00[ASN][1000 genomes]
rs6915105	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6916625	1.00[ASN][1000 genomes]
rs6925385	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6934750	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73781819	1.00[ASN][1000 genomes]
rs7738882	1.00[ASN][1000 genomes]
rs7741505	1.00[ASN][1000 genomes]
rs7746796	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7754527	0.85[AMR][1000 genomes]
rs7757254	0.91[ASN][1000 genomes]
rs9497313	1.00[ASN][1000 genomes]
rs9497314	1.00[ASN][1000 genomes]
rs9497318	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497320	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017166	chr6:145677071-145808448	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv604838	chr6:145709371-145841146	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv520619	chr6:145800915-145807907	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	n/a
4	esv2763962	chr6:145802158-145817051	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145803200-145805200	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr6:145803600-145804600	Enhancers	HMEC	breast
3	chr6:145803600-145804600	Enhancers	NHEK	skin
4	chr6:145803800-145804600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr6:145803800-145805600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr6:145803800-145805600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr6:145803800-145806000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:145804000-145804800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr6:145804000-145805200	Enhancers	Hela-S3	cervix
10	chr6:145804200-145805200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:145804400-145805000	Enhancers	Muscle Satellite Cultured Cells	--
12	chr6:145804400-145805000	Enhancers	HUVEC	blood vessel

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