Variant report

Variant	rs11063198
Chromosome Location	chr12:4591351-4591352
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:46)

rs_ID	r²[population]
rs1029769	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10849083	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10849085	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10849086	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10849089	0.83[ASN][1000 genomes]
rs10849090	0.83[ASN][1000 genomes]
rs11063179	0.82[EUR][1000 genomes]
rs11063181	0.82[EUR][1000 genomes]
rs11063182	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11063187	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11063188	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11063189	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11063191	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11063193	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11063194	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11063195	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11063196	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11063197	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11063199	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11063202	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11063205	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11063206	0.83[ASN][1000 genomes]
rs11063207	0.83[ASN][1000 genomes]
rs11063213	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11063214	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11063215	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11063217	0.83[ASN][1000 genomes]
rs12366731	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12367035	0.83[ASN][1000 genomes]
rs2907494	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2907495	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2907498	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2907499	0.83[ASN][1000 genomes]
rs2909380	0.83[ASN][1000 genomes]
rs2909381	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2970808	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2970810	0.83[ASN][1000 genomes]
rs2970812	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2970818	0.83[ASN][1000 genomes]
rs4323977	0.83[ASN][1000 genomes]
rs60388479	0.83[ASN][1000 genomes]
rs61909580	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73037770	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7304949	0.83[ASN][1000 genomes]
rs9971700	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9971728	0.81[EUR][1000 genomes];0.83[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	nsv530520	chr12:3726841-4601757	Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv557123	chr12:4436632-4736569	Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:4586800-4591800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:4586800-4596400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr12:4587200-4597200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr12:4587200-4597200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr12:4588600-4592200	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr12:4590000-4596200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr12:4590200-4597600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr12:4590800-4631200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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