Variant report

Variant	rs10471153
Chromosome Location	chr4:69163394-69163395
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	chr4:69163114..69165945-chr4:69212940..69216263,3	K562	blood:

Variant related genes	Relation type
ENSG00000083896	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10003465	0.81[EUR][1000 genomes]
rs10005832	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10866204	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11131746	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11732554	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11735530	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12331971	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13121372	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13127027	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13145544	0.80[EUR][1000 genomes]
rs13148330	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1406695	0.88[EUR][1000 genomes]
rs1406696	0.88[EUR][1000 genomes]
rs17089240	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17089241	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1715086	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1730872	0.95[EUR][1000 genomes]
rs1730875	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1880183	0.95[EUR][1000 genomes]
rs1919905	0.89[EUR][1000 genomes]
rs1962172	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2140519	0.93[EUR][1000 genomes]
rs2319887	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34032921	0.88[EUR][1000 genomes]
rs34186169	0.87[EUR][1000 genomes]
rs34223548	0.88[EUR][1000 genomes]
rs34265565	0.83[EUR][1000 genomes]
rs34474886	0.81[EUR][1000 genomes]
rs34527218	0.88[EUR][1000 genomes]
rs34896019	0.88[EUR][1000 genomes]
rs35051311	0.87[EUR][1000 genomes]
rs4860292	0.89[EUR][1000 genomes]
rs4860927	0.91[EUR][1000 genomes]
rs4860932	0.86[EUR][1000 genomes]
rs4860933	0.88[EUR][1000 genomes]
rs4860934	0.88[EUR][1000 genomes]
rs4860935	0.85[EUR][1000 genomes]
rs62316204	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6552179	0.83[ASN][1000 genomes]
rs6822778	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7658151	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7671950	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7672364	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7678448	0.83[EUR][1000 genomes]
rs7696268	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs953794	1.00[ASN][1000 genomes]
rs953795	1.00[ASN][1000 genomes]
rs9990842	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9991215	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008084	chr4:68797598-69482831	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS 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	44 gene(s)	inside rSNPs	diseases
2	nsv537131	chr4:68797598-69482831	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	esv1806586	chr4:68943858-69592846	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv461546	chr4:69049643-69223057	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv594506	chr4:69049643-69223057	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv537132	chr4:69149648-69482831	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10471153	YTHDC1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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