Variant report

Variant	rs73753694
Chromosome Location	chr5:43944545-43944546
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	chr5:43944227..43945254-chr5:44332040..44333058,5	MCF-7	breast:
2	chr5:43943850..43945210-chr5:44332166..44333349,5	MCF-7	breast:

Extended variants
information (count: 94 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs10461751	0.95[ASN][1000 genomes]
rs13155063	0.92[ASN][1000 genomes]
rs13157839	0.82[ASN][1000 genomes]
rs13159468	0.83[ASN][1000 genomes]
rs13162787	0.95[ASN][1000 genomes]
rs13163941	0.83[ASN][1000 genomes]
rs13171334	0.95[ASN][1000 genomes]
rs13175096	0.83[ASN][1000 genomes]
rs13182333	0.95[ASN][1000 genomes]
rs13184580	0.95[ASN][1000 genomes]
rs13186056	0.95[ASN][1000 genomes]
rs13189575	0.83[ASN][1000 genomes]
rs34048286	0.95[ASN][1000 genomes]
rs34053815	0.96[ASN][1000 genomes]
rs34085387	0.95[ASN][1000 genomes]
rs34136561	0.95[ASN][1000 genomes]
rs34157568	0.83[ASN][1000 genomes]
rs34338792	0.95[ASN][1000 genomes]
rs34371282	0.95[ASN][1000 genomes]
rs34464981	0.93[ASN][1000 genomes]
rs34518294	0.95[ASN][1000 genomes]
rs34528370	0.83[ASN][1000 genomes]
rs34579696	0.83[ASN][1000 genomes]
rs34601610	0.83[ASN][1000 genomes]
rs34602870	0.83[ASN][1000 genomes]
rs34632546	0.90[ASN][1000 genomes]
rs34685647	0.91[ASN][1000 genomes]
rs34758083	0.95[ASN][1000 genomes]
rs34782313	0.95[ASN][1000 genomes]
rs34843393	0.83[ASN][1000 genomes]
rs35013918	0.95[ASN][1000 genomes]
rs35029702	0.94[ASN][1000 genomes]
rs35092969	0.83[ASN][1000 genomes]
rs35140592	0.91[ASN][1000 genomes]
rs35162434	0.95[ASN][1000 genomes]
rs35182890	0.95[ASN][1000 genomes]
rs35208539	0.95[ASN][1000 genomes]
rs35289692	0.93[ASN][1000 genomes]
rs35374202	0.95[ASN][1000 genomes]
rs35430857	0.95[ASN][1000 genomes]
rs35529195	0.83[ASN][1000 genomes]
rs35696398	0.90[ASN][1000 genomes]
rs35697247	0.95[ASN][1000 genomes]
rs35730404	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35789639	0.83[ASN][1000 genomes]
rs35792109	0.95[ASN][1000 genomes]
rs35798472	0.83[ASN][1000 genomes]
rs36030354	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs36030928	0.81[ASN][1000 genomes]
rs36062010	0.93[ASN][1000 genomes]
rs4354051	0.83[ASN][1000 genomes]
rs4543275	0.83[ASN][1000 genomes]
rs4563636	0.83[ASN][1000 genomes]
rs4597977	0.95[ASN][1000 genomes]
rs4615307	0.83[ASN][1000 genomes]
rs4866756	0.96[ASN][1000 genomes]
rs4866757	0.95[ASN][1000 genomes]
rs4866760	0.89[ASN][1000 genomes]
rs4866845	0.91[ASN][1000 genomes]
rs4866852	0.83[ASN][1000 genomes]
rs4866853	0.83[ASN][1000 genomes]
rs56337432	0.95[ASN][1000 genomes]
rs58731744	0.95[ASN][1000 genomes]
rs59751856	0.83[ASN][1000 genomes]
rs6451737	0.83[ASN][1000 genomes]
rs6451741	0.83[ASN][1000 genomes]
rs67443644	0.95[ASN][1000 genomes]
rs67991400	0.96[ASN][1000 genomes]
rs6859597	0.94[ASN][1000 genomes]
rs6860696	0.83[ASN][1000 genomes]
rs6864990	0.83[ASN][1000 genomes]
rs6870141	0.95[ASN][1000 genomes]
rs6882508	0.95[ASN][1000 genomes]
rs6885572	0.80[AFR][1000 genomes]
rs6887519	0.83[ASN][1000 genomes]
rs6888119	0.90[ASN][1000 genomes]
rs71631110	0.95[ASN][1000 genomes]
rs71631119	0.95[ASN][1000 genomes]
rs71631120	0.96[ASN][1000 genomes]
rs71631121	0.95[ASN][1000 genomes]
rs71631187	0.94[ASN][1000 genomes]
rs71631189	0.93[ASN][1000 genomes]
rs71633107	0.83[ASN][1000 genomes]
rs71633109	0.83[ASN][1000 genomes]
rs71633110	0.83[ASN][1000 genomes]
rs7714254	0.95[ASN][1000 genomes]
rs7721923	0.84[ASN][1000 genomes]
rs7730331	0.95[ASN][1000 genomes]
rs7731350	0.83[ASN][1000 genomes]
rs9800184	0.95[ASN][1000 genomes]
rs9800296	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2830374	chr5:43785548-44341631	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1019047	chr5:43939693-44301657	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv969953	chr5:43943510-43949010	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43942000-43946000	Weak transcription	Adipose Nuclei	Adipose

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