Variant report

Variant	rs61900607
Chromosome Location	chr11:105387125-105387126
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:105386392..105390271-chr11:105390610..105394046,5	K562	blood:
2	chr11:105385673..105387781-chr11:105388066..105390476,3	K562	blood:
3	chr11:105385111..105387374-chr11:105388976..105390591,2	K562	blood:
4	chr11:105384754..105389238-chr11:105390610..105395129,6	K562	blood:
5	chr11:105386174..105388454-chr11:105417790..105420775,3	K562	blood:
6	chr11:105371540..105374049-chr11:105386860..105389341,2	K562	blood:
7	chr11:105371540..105374603-chr11:105385340..105388360,3	K562	blood:
8	chr11:105352067..105353901-chr11:105385410..105387990,2	K562	blood:
9	chr11:105380496..105383732-chr11:105384771..105387994,4	K562	blood:

No data

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10160500	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10502048	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10895814	0.88[ASN][1000 genomes]
rs10895826	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1113611	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11226739	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11226748	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11601213	0.80[EUR][1000 genomes]
rs11603521	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11823120	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12270282	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12271138	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12277692	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17468921	0.81[EUR][1000 genomes]
rs1945956	0.80[EUR][1000 genomes]
rs1945958	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1945977	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2032412	0.90[ASN][1000 genomes]
rs2032413	0.90[ASN][1000 genomes]
rs4427540	0.80[EUR][1000 genomes]
rs4619125	0.80[EUR][1000 genomes]
rs55860203	0.80[EUR][1000 genomes]
rs55885845	0.90[ASN][1000 genomes]
rs55888831	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs55954762	0.80[EUR][1000 genomes]
rs56219931	0.80[EUR][1000 genomes]
rs61900598	0.81[EUR][1000 genomes]
rs61900606	0.81[EUR][1000 genomes]
rs7120172	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7121772	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7122612	0.81[EUR][1000 genomes]
rs7125326	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72986173	0.82[EUR][1000 genomes]
rs7924758	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7927980	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7935262	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7938098	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9651715	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9804516	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9988916	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9988917	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949337	chr11:104950007-105510193	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv556221	chr11:105243371-105392079	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:105385200-105387800	Active TSS	K562	blood
2	chr11:105386000-105387200	Active TSS	Placenta	Placenta

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