Variant report

No.	Distal block	Cell Line	Cell type
1	chr13:93040364..93042788-chr13:93045821..93048248,2	K562	blood:
2	chr13:93041866..93044276-chr13:93051654..93053677,3	K562	blood:
3	chr13:93026262..93028061-chr13:93041707..93043886,2	K562	blood:
4	chr13:93029774..93033381-chr13:93039131..93043022,5	K562	blood:
5	chr13:93026561..93029613-chr13:93041707..93044561,3	K562	blood:
6	chr13:93036860..93038900-chr13:93040380..93043819,4	K562	blood:

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]
rs12868999	1.00[CEU][hapmap];1.00[YRI][hapmap]
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:6 , 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	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
3	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
4	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
5	nsv900903	chr13:92999147-93043373	Enhancers ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93041600-93042600	Weak transcription	Fetal Lung	lung
2	chr13:93042000-93043200	Enhancers	Pancreatic Islets	Pancreatic Islet

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