Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:40376872..40378665-chr13:40381947..40384768,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11617586	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12020434	0.88[ASN][1000 genomes]
rs12857806	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12859245	0.87[ASN][1000 genomes]
rs34927174	0.82[ASN][1000 genomes]
rs4312181	0.84[ASN][1000 genomes]
rs4531603	0.90[ASN][1000 genomes]
rs4575406	0.86[JPT][hapmap]
rs4943700	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7317488	0.92[ASN][1000 genomes]
rs7335495	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7988955	0.85[AFR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9594367	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9594368	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9594373	0.82[JPT][hapmap]
rs9603618	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9603619	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9603620	0.90[ASN][1000 genomes]
rs9603621	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9603626	0.83[EUR][1000 genomes];0.92[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	nsv1054600	chr13:39801283-40545027	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1054797	chr13:40198744-40618428	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
3	nsv541755	chr13:40198744-40618428	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
4	nsv1040458	chr13:40249387-40638129	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:40378400-40384200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:40382400-40385000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr13:40382600-40404000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr13:40383800-40384400	Enhancers	Ovary	ovary
5	chr13:40383800-40385400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr13:40383800-40385800	Enhancers	Placenta	Placenta
7	chr13:40384000-40384200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr13:40384000-40384200	Enhancers	H9 Cell Line	embryonic stem cell
9	chr13:40384000-40384200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr13:40384000-40386000	Enhancers	Primary hematopoietic stem cells short term culture	blood

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