Variant report

No data

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

No.	Distal block	Cell Line	Cell type
1	chr2:182885247..182888264-chr2:182945298..182948359,3	MCF-7	breast:
2	chr2:182606478..182612379-chr2:182941539..182945973,8	MCF-7	breast:
3	chr2:182877550..182879445-chr2:182944540..182946964,2	MCF-7	breast:
4	chr2:182753389..182769521-chr2:182932013..182949608,79	MCF-7	breast:
5	chr2:182944117..182946257-chr2:182954795..182956782,2	MCF-7	breast:
6	chr2:182941653..182947128-chr2:182990854..182994247,10	MCF-7	breast:
7	chr2:182940136..182945901-chr2:182990915..182998605,17	MCF-7	breast:
8	chr2:182753988..182769660-chr2:182938612..182954194,58	MCF-7	breast:
9	chr2:182932067..182937899-chr2:182939888..182947237,17	MCF-7	breast:
10	chr2:182943683..182945595-chr2:183046138..183048424,2	MCF-7	breast:
11	chr2:182590275..182592284-chr2:182942786..182945570,2	MCF-7	breast:
12	chr2:182880158..182888359-chr2:182937576..182947086,29	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000260742	Chromatin interaction
ENSG00000138434	Chromatin interaction

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

rs_ID	r²[population]
rs10930986	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10930987	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1196146	0.81[EUR][1000 genomes]
rs1196147	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1196148	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1196149	0.90[EUR][1000 genomes]
rs1196151	0.91[EUR][1000 genomes]
rs1196154	0.93[EUR][1000 genomes]
rs1196174	0.92[EUR][1000 genomes]
rs13395058	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1921147	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1921148	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1963270	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4404233	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6710397	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6747009	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7561331	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7579701	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7603587	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs987787	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875477	chr2:182938377-183086478	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182942600-182945800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:182944400-182946000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr2:182944400-182946000	Weak transcription	Fetal Lung	lung
4	chr2:182945000-182945800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr2:182945200-182945600	Enhancers	Primary hematopoietic stem cells	blood

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