Variant report

Variant	rs73301278
Chromosome Location	chr7:12996028-12996029
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10254523	0.94[ASN][1000 genomes]
rs10479912	0.94[ASN][1000 genomes]
rs11765383	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs13236466	0.84[ASN][1000 genomes]
rs2024402	0.90[ASN][1000 genomes]
rs2192676	0.82[ASN][1000 genomes]
rs246826	0.89[ASN][1000 genomes]
rs246828	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs28478673	0.93[ASN][1000 genomes]
rs34044	0.88[ASN][1000 genomes]
rs34048	0.91[ASN][1000 genomes]
rs34049	0.91[ASN][1000 genomes]
rs34055	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs34061	0.82[ASN][1000 genomes]
rs34066	0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs34067	0.94[ASN][1000 genomes]
rs34068	0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs34076	0.84[ASN][1000 genomes]
rs34078	0.86[ASN][1000 genomes]
rs4721165	0.88[ASN][1000 genomes]
rs4721168	0.85[ASN][1000 genomes]
rs58455143	0.89[ASN][1000 genomes]
rs6969615	0.98[ASN][1000 genomes]
rs71525640	0.82[ASN][1000 genomes]
rs73301284	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932020	chr7:12676890-13239551	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv868830	chr7:12712753-13517417	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv606235	chr7:12781381-13205950	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1020568	chr7:12802640-13183737	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv464384	chr7:12907178-13077065	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv606238	chr7:12907178-13077065	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1029771	chr7:12927648-13153855	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv538736	chr7:12927648-13153855	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1026624	chr7:12963907-13123408	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv887642	chr7:12973609-13067198	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12991800-12997200	Weak transcription	NHEK	skin
2	chr7:12991800-13004400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:12992400-12997200	Weak transcription	K562	blood
4	chr7:12993600-13002400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr7:12994800-13010000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr7:12996000-12996200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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