Variant report

Variant	rs71494765
Chromosome Location	chr10:45755564-45755565
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	chr10:45501761..45504279-chr10:45755487..45758024,2	K562	blood:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1011388	0.90[ASN][1000 genomes]
rs1073450	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1073451	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10900192	0.90[ASN][1000 genomes]
rs1122801	0.90[ASN][1000 genomes]
rs11239400	0.86[ASN][1000 genomes]
rs11239406	0.87[ASN][1000 genomes]
rs11239411	0.84[ASN][1000 genomes]
rs11597509	0.88[ASN][1000 genomes]
rs1339748	0.86[ASN][1000 genomes]
rs1578205	0.87[ASN][1000 genomes]
rs1836467	0.85[ASN][1000 genomes]
rs1897891	0.85[ASN][1000 genomes]
rs1897892	0.85[ASN][1000 genomes]
rs2163190	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34650304	0.85[ASN][1000 genomes]
rs4643031	0.85[ASN][1000 genomes]
rs4948662	0.91[ASN][1000 genomes]
rs4948976	0.87[ASN][1000 genomes]
rs4948977	0.87[ASN][1000 genomes]
rs4948978	0.87[ASN][1000 genomes]
rs4948979	0.90[ASN][1000 genomes]
rs4948983	0.84[ASN][1000 genomes]
rs4948985	0.85[ASN][1000 genomes]
rs61852251	0.86[ASN][1000 genomes]
rs7079089	0.85[ASN][1000 genomes]
rs7099002	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7894766	0.88[ASN][1000 genomes]
rs7898089	0.90[ASN][1000 genomes]
rs7907957	0.87[ASN][1000 genomes]
rs7909803	0.90[ASN][1000 genomes]
rs7910028	0.90[ASN][1000 genomes]
rs7917466	0.87[ASN][1000 genomes]

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	esv2750897	chr10:45550145-45820136	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
2	nsv895105	chr10:45636867-45928822	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
3	nsv430166	chr10:45668894-46148794	Bivalent Enhancer Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv993428	chr10:45742877-46224333	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv947610	chr10:45752231-45769447	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45752200-45756200	Weak transcription	K562	blood
2	chr10:45752800-45761800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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