Variant report

Variant	rs1310099
Chromosome Location	chr11:25984217-25984218
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1025837	0.81[EUR][1000 genomes]
rs1025839	0.81[EUR][1000 genomes]
rs11029025	0.85[ASN][1000 genomes]
rs11602363	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1215897	0.94[ASN][1000 genomes]
rs12417956	0.81[EUR][1000 genomes]
rs1348166	0.80[EUR][1000 genomes]
rs1441491	0.86[ASN][1000 genomes]
rs1441494	0.81[EUR][1000 genomes]
rs1441510	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs167877	0.82[EUR][1000 genomes]
rs167878	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs179189	0.89[EUR][1000 genomes]
rs184494	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs184495	0.85[EUR][1000 genomes]
rs2249568	0.85[EUR][1000 genomes]
rs2249717	0.85[EUR][1000 genomes]
rs228189	0.90[EUR][1000 genomes]
rs228190	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2349603	0.81[EUR][1000 genomes]
rs3103399	0.92[ASN][1000 genomes]
rs328464	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs328466	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs328467	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs328468	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs328469	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs328470	0.94[ASN][1000 genomes]
rs328471	0.94[ASN][1000 genomes]
rs328484	0.89[EUR][1000 genomes]
rs328486	0.96[ASN][1000 genomes]
rs328487	0.85[EUR][1000 genomes]
rs328488	0.85[EUR][1000 genomes]
rs4291637	0.81[EUR][1000 genomes]
rs4922749	0.86[ASN][1000 genomes]
rs61885276	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61885280	0.85[EUR][1000 genomes]
rs7101988	0.81[EUR][1000 genomes]
rs7928222	0.83[EUR][1000 genomes]
rs894174	0.85[EUR][1000 genomes]
rs971386	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760599	chr11:25186984-26159450	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1046507	chr11:25469712-26111707	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv832091	chr11:25823826-26009887	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv469948	chr11:25859783-26026233	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1041778	chr11:25898574-26098141	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv897140	chr11:25905509-25991194	Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv467777	chr11:25959082-25985507	Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	inside rSNPs	diseases
8	nsv553898	chr11:25959082-25985507	Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	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	chr11:25974400-25989400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr11:25979400-25988600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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