Variant report

Variant	rs12868999
Chromosome Location	chr13:93026278-93026279
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr13:93024437..93027101-chr13:93028065..93030296,2	K562	blood:
2	chr13:93026262..93028061-chr13:93041707..93043886,2	K562	blood:
3	chr13:93013213..93015773-chr13:93023566..93027348,3	K562	blood:
4	chr13:93024752..93026535-chr13:93034305..93036660,2	K562	blood:

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs12853588	1.00[YRI][hapmap]
rs12854568	1.00[AFR][1000 genomes]
rs12864687	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs12865759	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs12868141	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs12869734	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12871110	1.00[AFR][1000 genomes]
rs12871876	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs12873529	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs12875735	1.00[AFR][1000 genomes]
rs12876085	1.00[AFR][1000 genomes]
rs12876767	1.00[AFR][1000 genomes]
rs12877104	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs12877979	1.00[AFR][1000 genomes]
rs34004765	1.00[AFR][1000 genomes]
rs34022722	1.00[AFR][1000 genomes]
rs34037601	1.00[AFR][1000 genomes]
rs34240704	1.00[AFR][1000 genomes]
rs34322289	1.00[AFR][1000 genomes]
rs34453614	1.00[AFR][1000 genomes]
rs34669502	1.00[AFR][1000 genomes]
rs34708656	1.00[AFR][1000 genomes]
rs34719909	1.00[AFR][1000 genomes]
rs35243013	1.00[AFR][1000 genomes]
rs35254585	1.00[AFR][1000 genomes]
rs35352976	1.00[AFR][1000 genomes]
rs35609677	1.00[AFR][1000 genomes]
rs35629298	1.00[AFR][1000 genomes]
rs35970869	1.00[AFR][1000 genomes]
rs36048472	1.00[AFR][1000 genomes]
rs36076510	1.00[AFR][1000 genomes]
rs71427554	1.00[AFR][1000 genomes]
rs71427573	1.00[AFR][1000 genomes]
rs7328919	1.00[CEU][hapmap]
rs9561028	1.00[CEU][hapmap]

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	esv2756005	chr13:92584199-93080799	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2753357	chr13:92903199-93026399	Enhancers ZNF genes & repeats Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1036835	chr13:92953101-93039812	Enhancers ZNF genes & repeats Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1050788	chr13:92953101-93045491	Enhancers Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1051394	chr13:92959102-93049128	Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1037815	chr13:92959102-93052008	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv456068	chr13:92961151-93038913	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv562727	chr13:92961151-93038913	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv900903	chr13:92999147-93043373	Enhancers ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv976254	chr13:93007578-93034690	Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv832680	chr13:93021114-93181489	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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