Variant report

Variant	rs58297157
Chromosome Location	chr7:125062059-125062060
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10464530	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10500113	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10500114	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1358145	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1358146	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1358147	0.95[EUR][1000 genomes]
rs1526409	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1526410	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1526411	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1582860	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17132915	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17132917	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17132919	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17148311	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17148343	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17148357	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17148380	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17148383	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17148384	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17148403	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17148405	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1820591	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1834819	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1834821	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28613697	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55819664	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55947662	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56003455	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56114081	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56229058	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58689916	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59642554	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60204000	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60526024	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6956995	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7779471	0.97[EUR][1000 genomes]
rs7789050	0.95[EUR][1000 genomes]
rs7808860	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9641766	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9641767	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422188	chr7:124782873-125254203	Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	esv2761087	chr7:124823624-125429662	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv464709	chr7:124921028-125068580	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv608345	chr7:124921028-125068580	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv889141	chr7:124935779-125072969	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv889142	chr7:124958806-125068580	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1028369	chr7:124967804-125508233	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv948720	chr7:124970772-125783434	Transcr. at gene 5' and 3' Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv889144	chr7:124977736-125068580	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv889145	chr7:124977736-125231999	Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv889146	chr7:124996787-125083020	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv1018428	chr7:125044642-125730775	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv831120	chr7:125044774-125207696	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region lncRNA	1 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	chr7:125060200-125063200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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