Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs12192768	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12199482	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs169098	0.80[EUR][1000 genomes]
rs197475	0.80[EUR][1000 genomes]
rs197476	0.82[EUR][1000 genomes]
rs197477	0.80[EUR][1000 genomes]
rs197482	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs197491	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3383	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs3850224	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3850225	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3900201	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4896592	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4896593	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs517096	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56146803	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57584479	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7349872	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9373358	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9376706	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9390022	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949088	chr6:142561402-143128849	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv830828	chr6:142970134-143116517	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:143048800-143052600	Weak transcription	Placenta	Placenta
2	chr6:143049400-143056600	Weak transcription	Esophagus	oesophagus
3	chr6:143049800-143073200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:143050000-143058200	Weak transcription	NHEK	skin
5	chr6:143050000-143061600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:143050400-143058000	Weak transcription	Pancreas	Pancrea
7	chr6:143050600-143058600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr6:143050800-143058600	Weak transcription	NHDF-Ad	bronchial
9	chr6:143051000-143053200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr6:143051000-143053200	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr6:143051000-143053800	Weak transcription	Primary T cells from cord blood	blood
12	chr6:143051200-143056600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr6:143051800-143053200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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