Variant report

Variant	rs806192
Chromosome Location	chr7:127252903-127252904
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:127251080..127253485-chr7:127255790..127257541,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000106331	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1090681	0.88[ASN][1000 genomes]
rs1090682	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1090683	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2073561	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs327510	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs327511	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs327512	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs327516	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs327521	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3735642	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3735644	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3757793	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs594141	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs67719649	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs698406	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs712697	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs712698	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs712699	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs712700	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs712701	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs712703	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs712704	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72607743	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs806193	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs806195	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs806196	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs806214	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs806215	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs806216	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs806218	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs806219	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs806220	0.82[ASN][1000 genomes]
rs806221	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs989099	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs989100	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831122	chr7:127143207-127357885	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv1022385	chr7:127246656-127971194	Weak transcription Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv539120	chr7:127246656-127971194	Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv1016143	chr7:127251359-127726762	Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 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	chr7:127249800-127259600	Weak transcription	Pancreas	Pancrea

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