Variant report

Variant	rs6833264
Chromosome Location	chr4:153072885-153072886
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	chr4:153071984..153073977-chr4:153076704..153078831,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10030518	0.96[ASN][1000 genomes]
rs11099843	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11721407	0.96[ASN][1000 genomes]
rs11721782	0.95[ASN][1000 genomes]
rs11726930	0.96[ASN][1000 genomes]
rs11727245	0.83[AMR][1000 genomes]
rs11727862	0.96[ASN][1000 genomes]
rs11733393	0.89[ASN][1000 genomes]
rs11733971	0.96[ASN][1000 genomes]
rs11734900	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11736628	1.00[ASN][1000 genomes]
rs11737156	1.00[ASN][1000 genomes]
rs13107968	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13112841	1.00[ASN][1000 genomes]
rs13131134	1.00[ASN][1000 genomes]
rs2406622	1.00[ASN][1000 genomes]
rs2406625	0.96[ASN][1000 genomes]
rs28531716	0.82[ASN][1000 genomes]
rs2897478	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34069606	0.96[ASN][1000 genomes]
rs34276148	1.00[ASN][1000 genomes]
rs34909306	1.00[ASN][1000 genomes]
rs35296212	0.96[ASN][1000 genomes]
rs4557238	0.96[ASN][1000 genomes]
rs56780740	0.93[ASN][1000 genomes]
rs61226564	0.96[ASN][1000 genomes]
rs6535839	0.96[ASN][1000 genomes]
rs6535840	0.96[ASN][1000 genomes]
rs6823091	0.96[ASN][1000 genomes]
rs6837375	0.96[ASN][1000 genomes]
rs6843947	0.96[ASN][1000 genomes]
rs6848307	0.86[ASN][1000 genomes]
rs7662581	1.00[ASN][1000 genomes]
rs7671283	0.92[ASN][1000 genomes]
rs7674458	1.00[ASN][1000 genomes]
rs7675252	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7675481	1.00[ASN][1000 genomes]
rs7682931	1.00[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	nsv880341	chr4:152861685-153110256	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv931416	chr4:152877808-153440553	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv880774	chr4:153035743-153121818	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6833264	RP11-18H21.1	cis	Whole Blood	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:153068600-153073600	Enhancers	Fetal Thymus	thymus
2	chr4:153068600-153077400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:153072400-153074800	Weak transcription	Thymus	Thymus
4	chr4:153072800-153075000	Weak transcription	Dnd41	blood

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