Variant report

Variant	rs1678675
Chromosome Location	chr6:38760114-38760115
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	chr6:38758290..38761178-chr6:38769985..38772516,2	K562	blood:

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs1018437	0.92[JPT][hapmap]
rs1157884	0.89[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1614699	1.00[CHB][hapmap];0.84[JPT][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1630487	0.97[ASN][1000 genomes]
rs1678638	0.86[JPT][hapmap]
rs1678657	1.00[CHB][hapmap];0.84[JPT][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1678667	0.92[ASN][1000 genomes]
rs1678669	0.89[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1678717	0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs1678718	0.92[JPT][hapmap];0.85[ASN][1000 genomes]
rs1678725	0.92[JPT][hapmap];0.85[ASN][1000 genomes]
rs1678727	0.82[ASN][1000 genomes]
rs1678742	0.92[JPT][hapmap]
rs1738184	0.92[JPT][hapmap]
rs1738192	0.89[CEU][hapmap];0.86[JPT][hapmap];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1738203	0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs1738232	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1738236	1.00[ASN][1000 genomes]
rs1738238	0.95[ASN][1000 genomes]
rs1738239	0.86[CHB][hapmap];0.92[JPT][hapmap];0.95[ASN][1000 genomes]
rs1738240	0.86[CHB][hapmap];0.86[JPT][hapmap];0.95[ASN][1000 genomes]
rs1738241	0.86[JPT][hapmap];0.92[ASN][1000 genomes]
rs1738243	0.89[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1738247	0.86[CHB][hapmap];0.92[JPT][hapmap];0.97[ASN][1000 genomes]
rs1738263	1.00[CHB][hapmap];0.84[JPT][hapmap];0.95[ASN][1000 genomes]
rs2395709	0.85[JPT][hapmap]
rs2746170	0.86[CHB][hapmap]
rs4286777	0.91[JPT][hapmap]
rs4380739	0.85[JPT][hapmap]
rs4386804	0.86[JPT][hapmap]
rs4391252	0.92[JPT][hapmap]
rs4443498	0.86[JPT][hapmap]
rs4571559	0.86[JPT][hapmap]
rs4590258	0.86[JPT][hapmap]
rs4711558	0.92[JPT][hapmap]
rs4714193	0.86[JPT][hapmap]
rs6458080	0.92[JPT][hapmap]
rs6458081	0.86[JPT][hapmap]
rs6931736	0.86[JPT][hapmap]
rs761348	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs769064	0.86[CHB][hapmap]
rs862422	0.92[JPT][hapmap]
rs862425	0.92[JPT][hapmap]
rs862427	0.89[CEU][hapmap];0.92[JPT][hapmap]
rs9296265	0.92[JPT][hapmap]
rs9357290	0.92[JPT][hapmap]
rs9366982	0.86[JPT][hapmap]
rs9369089	0.86[JPT][hapmap]
rs9380789	0.92[JPT][hapmap]
rs9380796	0.86[JPT][hapmap]
rs9380798	0.86[JPT][hapmap]
rs9380799	0.86[JPT][hapmap]
rs9394547	0.86[JPT][hapmap]
rs9394550	0.92[JPT][hapmap]
rs982705	0.92[JPT][hapmap];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv885817	chr6:38036420-39019503	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv830642	chr6:38645056-38800657	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv830643	chr6:38726675-38905589	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv462915	chr6:38728142-38773293	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv602959	chr6:38728142-38786528	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv470814	chr6:38728142-38790149	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv462916	chr6:38747770-38782401	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv602960	chr6:38747770-38782401	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38751800-38763400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr6:38754600-38764000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:38758200-38763400	Weak transcription	HUVEC	blood vessel
4	chr6:38759800-38760200	Weak transcription	K562	blood

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