Variant report

Variant	rs4656779
Chromosome Location	chr1:170482533-170482534
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:170481966..170484499-chr1:170501498..170503077,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000231407	Chromatin interaction

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs10157476	0.80[AFR][1000 genomes]
rs10733056	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10753810	0.81[AFR][1000 genomes]
rs10753814	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10753815	0.92[ASW][hapmap];0.97[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10800527	0.83[ASW][hapmap];0.88[LWK][hapmap];0.95[MKK][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes]
rs10919425	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10919434	1.00[AMR][1000 genomes]
rs12062348	1.00[AMR][1000 genomes]
rs12072089	1.00[AMR][1000 genomes]
rs12087798	1.00[AMR][1000 genomes]
rs12088253	1.00[AMR][1000 genomes]
rs12116909	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1333133	0.92[ASW][hapmap];0.97[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1333142	0.96[YRI][hapmap]
rs1333146	0.82[AFR][1000 genomes]
rs1333150	0.92[AFR][1000 genomes]
rs1333151	0.84[AFR][1000 genomes]
rs1333152	0.80[AFR][1000 genomes]
rs1333153	0.84[AFR][1000 genomes]
rs1333154	0.84[AFR][1000 genomes]
rs1333155	0.96[AFR][1000 genomes]
rs1333156	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1412891	0.82[AFR][1000 genomes]
rs1412892	0.96[YRI][hapmap];0.88[AFR][1000 genomes]
rs1412893	0.88[AFR][1000 genomes]
rs1412894	0.80[AFR][1000 genomes]
rs1412895	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1537390	0.96[YRI][hapmap]
rs1537395	0.88[YRI][hapmap];0.82[AFR][1000 genomes]
rs1537397	0.92[ASW][hapmap];0.97[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1572026	0.84[AFR][1000 genomes]
rs1572027	0.82[AFR][1000 genomes]
rs1576979	0.83[AFR][1000 genomes]
rs1576980	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1831756	0.84[AFR][1000 genomes]
rs1855221	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1928716	0.96[YRI][hapmap]
rs1930632	1.00[MKK][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs1930633	0.84[AFR][1000 genomes]
rs1930634	0.84[AFR][1000 genomes]
rs1970116	0.80[AFR][1000 genomes]
rs2104918	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2150029	0.92[ASW][hapmap];0.97[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2151333	0.81[AFR][1000 genomes]
rs2225322	0.92[ASW][hapmap];0.97[LWK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2421325	0.83[ASW][hapmap];0.86[LWK][hapmap];0.90[MKK][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes]
rs2901401	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3936919	0.82[AFR][1000 genomes]
rs3980839	0.92[AFR][1000 genomes]
rs4233350	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4325194	0.88[AFR][1000 genomes]
rs4402174	0.94[AFR][1000 genomes]
rs4415629	0.90[AFR][1000 genomes]
rs4469769	0.84[AFR][1000 genomes]
rs4603185	0.81[AFR][1000 genomes]
rs4656769	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4656771	0.82[AFR][1000 genomes]
rs4656775	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4656777	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4656783	0.89[AFR][1000 genomes]
rs57462154	1.00[AMR][1000 genomes]
rs57674813	1.00[AMR][1000 genomes]
rs6427248	0.85[AFR][1000 genomes]
rs6427249	0.85[AFR][1000 genomes]
rs6427255	0.84[AFR][1000 genomes]
rs6427260	0.83[ASW][hapmap];0.85[LWK][hapmap];0.95[MKK][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes]
rs6427261	0.83[ASW][hapmap];0.88[LWK][hapmap];0.95[MKK][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes]
rs6657164	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6660575	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6664037	0.95[YRI][hapmap];0.92[AFR][1000 genomes]
rs6667304	0.91[AFR][1000 genomes]
rs6669308	0.83[ASW][hapmap];0.88[LWK][hapmap];0.95[MKK][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes]
rs6670724	0.98[AFR][1000 genomes]
rs6671312	0.96[YRI][hapmap];0.88[AFR][1000 genomes]
rs6676081	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6680083	1.00[AMR][1000 genomes]
rs6693763	0.83[ASW][hapmap];0.88[LWK][hapmap];0.90[MKK][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes]
rs6698637	0.81[AFR][1000 genomes]
rs6699057	0.81[AFR][1000 genomes]
rs6701004	0.84[AFR][1000 genomes]
rs6701218	0.92[YRI][hapmap];0.91[AFR][1000 genomes]
rs6703801	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7523665	0.89[AFR][1000 genomes]
rs7531125	0.92[ASW][hapmap];0.97[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7538125	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7548443	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7553254	0.96[YRI][hapmap];0.90[AFR][1000 genomes]
rs9651042	0.81[AFR][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	nsv872543	chr1:170171083-170674903	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv533915	chr1:170258766-170725296	Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:170481200-170482800	Enhancers	Dnd41	blood
2	chr1:170482200-170482600	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr1:170482400-170482600	Enhancers	Psoas Muscle	Psoas
4	chr1:170482400-170482800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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