Variant report

Variant	rs7910314
Chromosome Location	chr10:56004457-56004458
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10218915	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs11004148	1.00[CEU][hapmap]
rs11004151	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs11004166	1.00[CEU][hapmap];0.82[YRI][hapmap]
rs11004175	1.00[CEU][hapmap]
rs12240793	1.00[EUR][1000 genomes]
rs12240800	1.00[EUR][1000 genomes]
rs12242872	1.00[CEU][hapmap]
rs12245058	1.00[CEU][hapmap]
rs12245249	1.00[CEU][hapmap]
rs12248220	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs12250056	1.00[EUR][1000 genomes]
rs12252710	1.00[EUR][1000 genomes]
rs12252904	1.00[EUR][1000 genomes]
rs12255610	1.00[CEU][hapmap]
rs12260244	1.00[CEU][hapmap]
rs12260476	1.00[CEU][hapmap]
rs12261438	1.00[CEU][hapmap]
rs12261807	1.00[EUR][1000 genomes]
rs12268918	1.00[CEU][hapmap]
rs7069137	1.00[CEU][hapmap]
rs7077036	0.89[EUR][1000 genomes]
rs7086633	1.00[CEU][hapmap]
rs7090842	1.00[CEU][hapmap]
rs713274	1.00[CEU][hapmap]
rs7896210	1.00[CEU][hapmap]
rs7899424	1.00[EUR][1000 genomes]
rs7899428	1.00[EUR][1000 genomes]
rs7902567	1.00[EUR][1000 genomes]
rs7902932	1.00[EUR][1000 genomes]
rs7906179	1.00[EUR][1000 genomes]
rs7911444	1.00[CEU][hapmap];0.94[YRI][hapmap]
rs7913738	1.00[EUR][1000 genomes]
rs7915325	1.00[EUR][1000 genomes]
rs7915552	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7918079	1.00[EUR][1000 genomes]
rs7919046	1.00[CEU][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv8667	chr10:55803106-56022647	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv870252	chr10:55823123-56029435	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv948730	chr10:55845301-56093271	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1035173	chr10:55847066-56005288	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv430232	chr10:55883194-56027294	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2829924	chr10:55906112-56038831	Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1054364	chr10:55925471-56196447	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv540633	chr10:55925471-56196447	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv20105	chr10:55939729-56047721	ZNF genes & repeats Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv467215	chr10:55943184-56019194	Enhancers ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv550951	chr10:55943184-56019194	Active TSS ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7910314	MAP1B	trans	brain	seeQTL

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

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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