Variant report

Variant	rs7199772
Chromosome Location	chr16:47053737-47053738
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:47005161..47009239-chr16:47050620..47053908,8	MCF-7	breast:
2	chr16:47052300..47054787-chr16:48417459..48419848,2	K562	blood:

Variant related genes	Relation type
ENSG00000261173	Chromatin interaction
ENSG00000069345	Chromatin interaction
ENSG00000196470	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10459877	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11247542	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11247543	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11859515	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12445492	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12447719	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12596824	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12719759	0.85[EUR][1000 genomes]
rs12925296	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1362406	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1376734	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1551188	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1894886	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1978336	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2058673	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2341648	0.97[EUR][1000 genomes]
rs35405784	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4577108	0.97[EUR][1000 genomes]
rs4625742	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4966781	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4966794	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4966795	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4966800	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4967664	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4967696	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4967724	0.83[EUR][1000 genomes]
rs4967739	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62059134	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7189628	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7199379	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7202325	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7203206	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8046142	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8047353	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8052160	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8054039	0.92[EUR][1000 genomes]
rs8058144	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8058714	0.83[EUR][1000 genomes]
rs8060193	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9745921	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9923192	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9925290	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9925525	0.90[EUR][1000 genomes]
rs9927843	1.00[EUR][1000 genomes];0.83[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	nsv1059456	chr16:46463770-47307580	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
2	nsv1066115	chr16:46463770-47318415	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
3	nsv1056328	chr16:47011193-47172862	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 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	chr16:47048400-47067200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:47050800-47063200	Weak transcription	Right Atrium	heart
3	chr16:47051600-47053800	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr16:47053000-47054000	Weak transcription	Primary B cells from cord blood	blood
5	chr16:47053600-47054000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr16:47053600-47057400	Weak transcription	GM12878-XiMat	blood

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