Variant report

Variant	rs12550701
Chromosome Location	chr8:110027057-110027058
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs10505127	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs12156210	0.97[ASN][1000 genomes]
rs12375395	0.95[ASN][1000 genomes]
rs12543195	0.98[ASN][1000 genomes]
rs12543567	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12545538	0.98[ASN][1000 genomes]
rs12679431	0.97[ASN][1000 genomes]
rs13251349	0.97[ASN][1000 genomes]
rs13256422	0.97[ASN][1000 genomes]
rs13269540	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs13274272	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs13274565	0.90[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs13274898	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs17520	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34080186	0.91[ASN][1000 genomes]
rs4236798	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4236799	0.96[ASN][1000 genomes]
rs4236800	0.96[ASN][1000 genomes]
rs4276659	0.97[ASN][1000 genomes]
rs4292662	0.97[ASN][1000 genomes]
rs4292663	0.95[ASN][1000 genomes]
rs4316127	0.96[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs4319061	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4349964	0.96[ASN][1000 genomes]
rs4370503	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4428649	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4442116	0.98[ASN][1000 genomes]
rs4457304	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4464938	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4469428	0.96[ASN][1000 genomes]
rs4480098	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4484661	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4510830	0.98[ASN][1000 genomes]
rs4531025	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4538846	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4556069	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4557674	0.98[ASN][1000 genomes]
rs4567008	0.97[ASN][1000 genomes]
rs4577927	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4579501	0.95[ASN][1000 genomes]
rs4585725	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4620260	0.90[ASN][1000 genomes]
rs4631432	0.90[ASN][1000 genomes]
rs4645537	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4645538	0.98[ASN][1000 genomes]
rs4734187	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4734188	0.98[ASN][1000 genomes]
rs4734189	0.95[ASN][1000 genomes]
rs4735082	0.98[ASN][1000 genomes]
rs4735083	0.98[ASN][1000 genomes]
rs4735084	0.97[ASN][1000 genomes]
rs4735090	0.91[ASN][1000 genomes]
rs55812898	0.85[ASN][1000 genomes]
rs6469215	0.98[ASN][1000 genomes]
rs6469216	0.98[ASN][1000 genomes]
rs6469217	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6469219	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6469220	0.96[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs6469221	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6469223	0.90[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs6469224	0.91[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6469227	0.98[ASN][1000 genomes]
rs6981930	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6982425	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6987636	0.97[ASN][1000 genomes]
rs6990759	0.88[ASN][1000 genomes]
rs7001089	0.98[ASN][1000 genomes]
rs7004855	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7006400	0.89[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7007614	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7007733	0.94[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs7007742	0.97[ASN][1000 genomes]
rs7010190	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7012445	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7012614	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7463680	0.98[ASN][1000 genomes]
rs7465417	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7814973	0.96[ASN][1000 genomes]
rs7816859	0.98[ASN][1000 genomes]
rs7817020	0.95[ASN][1000 genomes]
rs7817222	0.95[ASN][1000 genomes]
rs7818891	0.93[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7819184	0.85[ASN][1000 genomes]
rs7823377	0.82[ASN][1000 genomes]
rs7823487	0.88[ASN][1000 genomes]
rs7827721	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7830847	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7834396	0.97[ASN][1000 genomes]
rs9643041	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9643042	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9643043	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[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	nsv1022273	chr8:110026712-110146600	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv539715	chr8:110026712-110146600	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr8:110023000-110028800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr8:110026800-110027200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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