Variant report

Variant	rs73311099
Chromosome Location	chr8:91807056-91807057
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:91805114..91806648-chr8:91807056..91808922,2	MCF-7	breast:
2	chr8:91806784..91808762-chr8:91842153..91844189,2	MCF-7	breast:
3	chr8:91799742..91802309-chr8:91804087..91807795,3	MCF-7	breast:
4	chr8:91805846..91807806-chr8:91868153..91870777,2	MCF-7	breast:
5	chr8:91655695..91657922-chr8:91806739..91808308,2	K562	blood:

Variant related genes	Relation type
ENSG00000180694	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10504897	0.83[AMR][1000 genomes]
rs10504899	0.87[AMR][1000 genomes]
rs10504900	0.83[AMR][1000 genomes]
rs10504902	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11994903	0.82[ASN][1000 genomes]
rs11997330	0.82[ASN][1000 genomes]
rs12114679	0.82[ASN][1000 genomes]
rs16905319	0.87[AMR][1000 genomes]
rs16905331	0.83[AMR][1000 genomes]
rs16905427	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs16905437	0.82[ASN][1000 genomes]
rs2202392	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4389891	0.82[ASN][1000 genomes]
rs4443621	0.82[ASN][1000 genomes]
rs55997084	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56201758	0.82[ASN][1000 genomes]
rs56216319	0.82[ASN][1000 genomes]
rs56284988	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56834391	0.82[ASN][1000 genomes]
rs56895928	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58037813	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs58942247	0.82[ASN][1000 genomes]
rs59253454	0.83[AMR][1000 genomes]
rs59416504	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60664481	0.83[AMR][1000 genomes]
rs60690249	0.83[AMR][1000 genomes]
rs61163578	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61312544	0.83[AMR][1000 genomes]
rs61441737	0.83[AMR][1000 genomes]
rs6471253	0.83[AMR][1000 genomes]
rs7011031	0.83[AMR][1000 genomes]
rs7013400	0.87[AMR][1000 genomes]
rs73307288	0.83[AMR][1000 genomes]
rs73311066	0.83[AMR][1000 genomes]
rs73311068	0.83[AMR][1000 genomes]
rs73311083	0.83[AMR][1000 genomes]
rs73311086	0.83[AMR][1000 genomes]
rs73311089	0.83[AMR][1000 genomes]
rs73311093	0.87[AMR][1000 genomes]
rs73313059	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73313067	0.82[ASN][1000 genomes]
rs73313090	0.82[ASN][1000 genomes]
rs7815900	0.87[AMR][1000 genomes]
rs7818878	0.80[AMR][1000 genomes]
rs7838907	0.82[ASN][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	nsv1028628	chr8:91680968-92418954	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv539672	chr8:91680968-92418954	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv1034104	chr8:91723213-91847147	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv539673	chr8:91723213-91847147	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91803000-91807200	Active TSS	Brain Inferior Temporal Lobe	brain
2	chr8:91805200-91807200	Active TSS	Fetal Brain Female	brain
3	chr8:91805800-91807600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr8:91805800-91807800	Enhancers	Brain Substantia Nigra	brain
5	chr8:91806000-91810600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr8:91806400-91807200	Weak transcription	Brain Angular Gyrus	brain
7	chr8:91806800-91807200	Flanking Active TSS	Brain Hippocampus Middle	brain
8	chr8:91806800-91807200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
9	chr8:91806800-91807400	Flanking Active TSS	Brain Anterior Caudate	brain
10	chr8:91807000-91808000	Enhancers	Brain Cingulate Gyrus	brain

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