Variant report

Variant	rs16890967
Chromosome Location	chr6:25718273-25718274
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	chr6:25717832..25722141-chr6:25722443..25725099,3	K562	blood:
2	chr6:25717672..25720763-chr6:26020986..26022680,3	K562	blood:

Variant related genes	Relation type
ENSG00000196176	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1165194	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1165197	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1165198	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16891011	0.83[EUR][1000 genomes]
rs17341475	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1892252	1.00[JPT][hapmap]
rs2154220	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2154221	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2762352	1.00[CHB][hapmap];0.82[JPT][hapmap];0.92[ASN][1000 genomes]
rs34892514	1.00[ASN][1000 genomes]
rs34902660	0.92[ASN][1000 genomes]
rs3734525	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3734526	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4481423	1.00[JPT][hapmap]
rs59340721	1.00[ASN][1000 genomes]
rs59811281	0.83[EUR][1000 genomes]
rs61120493	1.00[ASN][1000 genomes]
rs61242778	1.00[ASN][1000 genomes]
rs6900548	1.00[CHB][hapmap]
rs6904823	0.92[ASN][1000 genomes]
rs6909034	0.92[ASN][1000 genomes]
rs6913042	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6928027	0.84[ASN][1000 genomes]
rs6930176	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7738813	0.83[EUR][1000 genomes]
rs7738984	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7748953	0.83[EUR][1000 genomes]
rs9348693	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv883488	chr6:25592489-25731691	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
4	nsv427747	chr6:25641380-25908218	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv526061	chr6:25708714-25725481	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25717400-25726600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:25717800-25718400	Enhancers	HepG2	liver
3	chr6:25718200-25718400	Enhancers	Fetal Brain Male	brain

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