Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:89196233..89199192-chr8:89205240..89207551,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10091022	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10104620	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10110977	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10113080	0.93[EUR][1000 genomes]
rs13256568	0.93[EUR][1000 genomes]
rs13261169	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13264048	0.92[EUR][1000 genomes]
rs13439559	0.93[EUR][1000 genomes]
rs16879913	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28542805	0.81[ASN][1000 genomes]
rs28589951	0.81[ASN][1000 genomes]
rs28639477	0.81[ASN][1000 genomes]
rs28649468	0.93[EUR][1000 genomes]
rs28678551	0.93[EUR][1000 genomes]
rs28730305	0.81[ASN][1000 genomes]
rs28904614	0.93[EUR][1000 genomes]
rs28904635	1.00[ASN][1000 genomes]
rs6469298	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7357573	0.93[EUR][1000 genomes]
rs7357575	0.93[EUR][1000 genomes]
rs7357576	0.93[EUR][1000 genomes]
rs7821734	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs939280	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029898	chr8:88837956-89606641	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1030028	chr8:89060085-89733470	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1019111	chr8:89186908-89475460	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:89160800-89217200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:89177200-89214400	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr8:89177200-89216400	Weak transcription	Brain Germinal Matrix	brain
4	chr8:89195000-89219200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr8:89195800-89210600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:89196600-89214200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr8:89196800-89214800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr8:89198800-89207000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr8:89200400-89206600	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr8:89201200-89218000	Weak transcription	Fetal Lung	lung
11	chr8:89203200-89211000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr8:89203400-89206400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr8:89204000-89219600	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr8:89204200-89217200	Weak transcription	NH-A	brain

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