Variant report

Variant	rs7670139
Chromosome Location	chr4:143779269-143779270
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:143766691..143769165-chr4:143778080..143780463,3	MCF-7	breast:
2	chr4:143777512..143779890-chr4:144104610..144106802,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000109452	Chromatin interaction
ENSG00000250326	Chromatin interaction
ENSG00000170185	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11100761	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11939835	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13112916	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13122287	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13145724	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1441411	0.86[ASN][1000 genomes]
rs1441417	0.81[ASN][1000 genomes]
rs1441418	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1444950	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17016873	0.81[ASN][1000 genomes]
rs1992652	0.83[ASN][1000 genomes]
rs2218240	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28416530	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2874907	0.81[ASN][1000 genomes]
rs4575951	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4690728	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4690730	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs60263370	0.83[ASN][1000 genomes]
rs6537127	0.88[ASN][1000 genomes]
rs6537130	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6811022	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6813785	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6824743	0.81[ASN][1000 genomes]
rs6831204	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6839158	0.86[ASN][1000 genomes]
rs6846609	0.81[ASN][1000 genomes]
rs6852412	0.81[ASN][1000 genomes]
rs72615963	0.87[ASN][1000 genomes]
rs72728700	0.83[ASN][1000 genomes]
rs72730409	0.85[ASN][1000 genomes]
rs73850583	0.85[ASN][1000 genomes]
rs7660533	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7668263	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7685997	0.83[ASN][1000 genomes]
rs877032	0.81[ASN][1000 genomes]
rs9994364	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[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	nsv880174	chr4:143639498-143848024	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr4:143768600-143781200	Weak transcription	Psoas Muscle	Psoas
2	chr4:143777600-143779600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr4:143779000-143780800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr4:143779200-143779600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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