Variant report

Variant	rs7667627
Chromosome Location	chr4:150835787-150835788
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:150835531..150836236-chr4:150901791..150902666,2	MCF-7	breast:
2	chr4:150835279..150836290-chr4:150844620..150845340,3	MCF-7	breast:
3	chr4:150835352..150836296-chr4:151130289..151131265,2	K562	blood:

Variant related genes	Relation type
ENSG00000238721	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10015292	0.81[AMR][1000 genomes]
rs10021417	0.81[AMR][1000 genomes]
rs10023988	0.81[AMR][1000 genomes]
rs10030973	0.81[AMR][1000 genomes]
rs10032786	0.87[AMR][1000 genomes]
rs10213081	0.87[AMR][1000 genomes]
rs11932683	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs1394846	0.87[AMR][1000 genomes]
rs17026476	0.81[AMR][1000 genomes]
rs17026559	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17026577	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2359689	0.81[AMR][1000 genomes]
rs28390223	0.81[AMR][1000 genomes]
rs28419623	0.87[AMR][1000 genomes]
rs28461843	0.81[AMR][1000 genomes]
rs28533652	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs28566505	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28695593	0.81[AMR][1000 genomes]
rs28703191	0.81[AMR][1000 genomes]
rs28709180	0.87[AMR][1000 genomes]
rs4594705	0.81[AMR][1000 genomes]
rs4835596	0.87[AMR][1000 genomes]
rs4835603	0.81[AMR][1000 genomes]
rs4835606	0.86[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6824353	0.87[AMR][1000 genomes]
rs6831721	0.81[AMR][1000 genomes]
rs73857778	0.87[AMR][1000 genomes]
rs73857791	0.81[AMR][1000 genomes]
rs73857792	0.82[AMR][1000 genomes]
rs73857798	0.81[AMR][1000 genomes]
rs73859805	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7655327	0.87[AMR][1000 genomes]
rs7665522	0.81[AMR][1000 genomes]
rs7677933	0.81[AMR][1000 genomes]
rs7684559	1.00[CEU][hapmap];0.80[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs7687723	1.00[CEU][hapmap]
rs7690612	0.81[AMR][1000 genomes]
rs7692136	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9991476	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9998271	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026797	chr4:150246932-151217137	Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1016169	chr4:150670127-150903827	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv537299	chr4:150670127-150903827	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv880254	chr4:150712923-150852782	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv880255	chr4:150777012-150874830	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv932022	chr4:150831733-151419552	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:150833600-150835800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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