Variant report

Variant	rs7926713
Chromosome Location	chr11:86474274-86474275
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:86472937..86474717-chr11:86478043..86479834,2	MCF-7	breast:
2	chr11:86472552..86476130-chr11:86481757..86485497,4	MCF-7	breast:
3	chr11:86471960..86474336-chr11:86510433..86512699,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000150687	Chromatin interaction

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs1075702	0.81[ASN][1000 genomes]
rs10792875	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10898534	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11234783	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11234795	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11234809	0.84[ASN][1000 genomes]
rs11601553	0.82[ASN][1000 genomes]
rs12361769	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12366016	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12576018	0.87[ASN][1000 genomes]
rs12797648	0.82[ASN][1000 genomes]
rs12802848	0.84[ASN][1000 genomes]
rs12809023	0.82[ASN][1000 genomes]
rs17211926	0.81[ASN][1000 genomes]
rs17819068	0.95[ASN][1000 genomes]
rs1939117	0.83[ASN][1000 genomes]
rs2433438	0.80[ASN][1000 genomes]
rs2513018	0.81[ASN][1000 genomes]
rs34833002	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35902217	0.83[ASN][1000 genomes]
rs36061072	0.83[ASN][1000 genomes]
rs4128368	0.82[ASN][1000 genomes]
rs4245426	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4245427	0.92[ASN][1000 genomes]
rs4269941	0.84[ASN][1000 genomes]
rs4307743	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4450192	0.96[ASN][1000 genomes]
rs4495915	0.84[ASN][1000 genomes]
rs4570601	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4943957	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4943958	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4943959	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4943960	0.92[ASN][1000 genomes]
rs4944629	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4944630	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4944631	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4944632	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4944633	0.93[ASN][1000 genomes]
rs4944634	0.92[ASN][1000 genomes]
rs55646317	0.82[ASN][1000 genomes]
rs58823830	0.87[ASN][1000 genomes]
rs58976693	0.82[ASN][1000 genomes]
rs59850783	0.92[ASN][1000 genomes]
rs60023003	0.92[ASN][1000 genomes]
rs61690902	0.93[ASN][1000 genomes]
rs61707378	0.82[ASN][1000 genomes]
rs6592315	0.83[ASN][1000 genomes]
rs7105467	0.85[ASN][1000 genomes]
rs7120185	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7120320	0.81[ASN][1000 genomes]
rs7123349	0.83[ASN][1000 genomes]
rs7126492	0.82[ASN][1000 genomes]
rs744292	0.82[ASN][1000 genomes]
rs7926235	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7926946	0.81[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs7927257	0.81[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs7927479	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7940201	0.81[ASN][1000 genomes]
rs7942344	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7948063	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7950776	0.81[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs7951582	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[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	nsv1044081	chr11:86133641-86868560	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv541118	chr11:86133641-86868560	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv428263	chr11:86357990-86508480	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1049157	chr11:86409059-86504155	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv521505	chr11:86438115-86515072	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv468775	chr11:86453415-86480716	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	nsv555705	chr11:86453415-86480716	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
8	esv2756074	chr11:86456552-86729552	Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86456600-86478000	Weak transcription	Aorta	Aorta
2	chr11:86461400-86479600	Weak transcription	Psoas Muscle	Psoas
3	chr11:86471600-86474400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:86472800-86474400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr11:86473200-86475200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr11:86473600-86480200	Weak transcription	A549	lung
7	chr11:86473800-86475800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr11:86473800-86476200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr11:86473800-86479600	Weak transcription	Left Ventricle	heart
10	chr11:86473800-86480000	Weak transcription	HSMMtube	muscle
11	chr11:86473800-86480200	Weak transcription	Hela-S3	cervix
12	chr11:86473800-86480200	Weak transcription	Osteobl	bone
13	chr11:86474200-86475600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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