Variant report

Variant	rs73588367
Chromosome Location	chr6:147717046-147717047
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:147712099..147713762-chr6:147716673..147718995,2	K562	blood:
2	chr6:147703869..147707372-chr6:147716822..147719564,3	K562	blood:
3	chr6:147710173..147716177-chr6:147716262..147720570,6	K562	blood:
4	chr6:147716288..147718963-chr6:147719642..147723185,3	K562	blood:

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

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

rs_ID	r²[population]
rs61645687	1.00[AFR][1000 genomes]
rs73580488	1.00[AFR][1000 genomes]
rs73582506	1.00[AFR][1000 genomes]
rs73582513	1.00[AFR][1000 genomes]
rs73582518	1.00[AFR][1000 genomes]
rs73582522	1.00[AFR][1000 genomes]
rs73582523	1.00[AFR][1000 genomes]
rs73582531	1.00[AFR][1000 genomes]
rs73582532	1.00[AFR][1000 genomes]
rs73582537	1.00[AFR][1000 genomes]
rs73582601	1.00[AFR][1000 genomes]
rs73584513	1.00[AFR][1000 genomes]
rs73584514	1.00[AFR][1000 genomes]
rs73584535	1.00[AFR][1000 genomes]
rs73584536	1.00[AFR][1000 genomes]
rs73584537	1.00[AFR][1000 genomes]
rs73586317	1.00[AFR][1000 genomes]
rs73586354	1.00[AFR][1000 genomes]
rs73586356	1.00[AFR][1000 genomes]
rs73586357	1.00[AFR][1000 genomes]
rs73588331	0.87[AFR][1000 genomes]
rs73588335	1.00[AFR][1000 genomes]
rs73588338	1.00[AFR][1000 genomes]
rs73588355	1.00[AFR][1000 genomes]
rs73588385	1.00[AFR][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	nsv886752	chr6:147443480-147729477	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv886754	chr6:147539165-147729477	Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv604840	chr6:147539165-147730324	Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv886755	chr6:147577646-147729477	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv886756	chr6:147580697-147729477	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
6	nsv830839	chr6:147584914-147757264	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv886757	chr6:147591022-147729477	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
8	nsv886759	chr6:147686274-147764267	Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147680400-147721800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:147687800-147724600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr6:147704200-147717600	Weak transcription	Fetal Stomach	stomach
4	chr6:147707400-147718400	Weak transcription	K562	blood
5	chr6:147709800-147718600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr6:147715800-147721200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:147716600-147717400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:147716800-147717200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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