Variant report

Variant	rs6550755
Chromosome Location	chr3:23373175-23373176
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 104 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:98)

rs_ID	r²[population]
rs1013460	0.84[CHB][hapmap];0.86[JPT][hapmap]
rs1027379	0.82[CHB][hapmap];0.88[JPT][hapmap];0.83[ASN][1000 genomes]
rs1032499	0.85[JPT][hapmap]
rs11129113	0.83[ASN][1000 genomes]
rs11129116	0.84[CHB][hapmap];0.84[ASN][1000 genomes]
rs11708117	0.80[ASN][1000 genomes]
rs11708160	0.82[CEU][hapmap]
rs11708176	0.87[ASN][1000 genomes]
rs11715841	0.82[CEU][hapmap]
rs11717397	0.87[ASN][1000 genomes]
rs11720461	0.90[CHB][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes]
rs11916411	0.81[JPT][hapmap]
rs12330479	0.83[CHB][hapmap];0.89[JPT][hapmap]
rs12493361	0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs12496983	0.88[ASN][1000 genomes]
rs12497974	0.82[ASN][1000 genomes]
rs12629848	0.84[CHB][hapmap];0.86[JPT][hapmap]
rs13074192	0.89[CHB][hapmap];0.91[JPT][hapmap];0.84[ASN][1000 genomes]
rs13326048	0.86[JPT][hapmap]
rs1495131	0.84[ASN][1000 genomes]
rs1532355	0.82[ASN][1000 genomes]
rs1552930	0.90[CHB][hapmap];0.90[JPT][hapmap]
rs1692617	0.81[JPT][hapmap]
rs17012812	0.83[CHB][hapmap];0.90[JPT][hapmap]
rs17012869	0.84[CHB][hapmap];0.86[JPT][hapmap]
rs1874235	0.84[ASN][1000 genomes]
rs1973400	0.83[ASN][1000 genomes]
rs2055310	0.87[CEU][hapmap]
rs2133331	0.81[CEU][hapmap]
rs2172828	0.84[CHB][hapmap];0.86[JPT][hapmap]
rs2173460	0.82[CEU][hapmap]
rs2359759	0.90[JPT][hapmap]
rs3111311	0.81[CEU][hapmap];0.81[JPT][hapmap]
rs3817002	0.81[CEU][hapmap];0.86[JPT][hapmap]
rs4241512	0.89[ASN][1000 genomes]
rs4488778	0.81[ASN][1000 genomes]
rs4858062	0.84[CHB][hapmap];0.86[JPT][hapmap]
rs4858071	0.80[ASN][1000 genomes]
rs4858483	0.83[CHB][hapmap];0.90[JPT][hapmap]
rs4858491	0.90[ASN][1000 genomes]
rs4858492	0.88[ASN][1000 genomes]
rs4858496	0.84[CHB][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs4858497	0.83[CHB][hapmap];0.82[ASN][1000 genomes]
rs4858500	0.84[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs4858501	0.84[ASN][1000 genomes]
rs4858502	0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs4858504	0.90[ASN][1000 genomes]
rs4858506	0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs4858508	0.84[ASN][1000 genomes]
rs4858509	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6550746	0.87[CHB][hapmap];0.84[JPT][hapmap]
rs6550748	0.83[CHB][hapmap];0.90[JPT][hapmap]
rs6550756	0.82[ASN][1000 genomes]
rs6776424	0.81[JPT][hapmap]
rs6780723	0.82[JPT][hapmap]
rs6784195	0.86[JPT][hapmap]
rs6784771	0.81[JPT][hapmap]
rs6797907	0.81[CEU][hapmap];0.81[JPT][hapmap]
rs6804123	0.83[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs6805889	0.81[CEU][hapmap];0.85[CHB][hapmap];0.86[JPT][hapmap];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs716457	0.82[ASN][1000 genomes]
rs7613091	0.81[CEU][hapmap];0.90[JPT][hapmap]
rs7617072	0.83[CHB][hapmap];0.90[JPT][hapmap]
rs7631334	0.90[JPT][hapmap]
rs778468	0.86[JPT][hapmap]
rs778480	0.85[JPT][hapmap]
rs778494	0.86[JPT][hapmap]
rs778508	0.81[JPT][hapmap]
rs778523	0.82[JPT][hapmap]
rs9310715	0.83[CHB][hapmap];0.90[JPT][hapmap]
rs9809176	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs9816895	0.88[ASN][1000 genomes]
rs9822422	0.84[ASN][1000 genomes]
rs9825778	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs9826089	0.83[ASN][1000 genomes]
rs9826877	0.88[CHB][hapmap];0.95[JPT][hapmap]
rs9830388	0.81[CEU][hapmap]
rs9836787	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs9839738	0.88[CEU][hapmap];0.90[CHB][hapmap];0.91[JPT][hapmap];0.80[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9841123	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs9846398	0.89[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs9847027	0.84[CHB][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs9847958	0.89[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs9848077	0.84[CHB][hapmap];0.86[JPT][hapmap]
rs9849176	0.83[JPT][hapmap];0.83[ASN][1000 genomes]
rs9853489	0.89[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs9854148	0.82[ASN][1000 genomes]
rs9854590	0.89[CHB][hapmap];0.90[JPT][hapmap]
rs9859515	0.84[ASN][1000 genomes]
rs9859651	0.90[JPT][hapmap]
rs9861803	0.82[ASN][1000 genomes]
rs9864908	0.82[JPT][hapmap]
rs9865602	0.90[ASN][1000 genomes]
rs9873317	0.83[ASN][1000 genomes]
rs9874082	0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs9874519	0.82[ASN][1000 genomes]
rs9874822	0.84[ASN][1000 genomes]
rs9881332	0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014701	chr3:23257658-23416094	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv589947	chr3:23277838-23403943	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1002823	chr3:23277838-23623083	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv589948	chr3:23287141-23390221	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1004417	chr3:23318797-23389422	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1007373	chr3:23367952-23710331	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23357000-23378800	Weak transcription	Brain Angular Gyrus	brain
2	chr3:23367000-23378800	Weak transcription	HSMMtube	muscle
3	chr3:23367400-23391400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr3:23368000-23374400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr3:23368000-23374600	Weak transcription	NHEK	skin
6	chr3:23368000-23391000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr3:23371200-23374400	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr3:23371400-23378400	Weak transcription	Psoas Muscle	Psoas
9	chr3:23372000-23382000	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr3:23372200-23378200	Weak transcription	Brain Hippocampus Middle	brain
11	chr3:23372200-23383400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:23372600-23373200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr3:23372800-23373200	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr3:23373000-23373200	Enhancers	Brain Substantia Nigra	brain
15	chr3:23373000-23373200	Enhancers	Right Atrium	heart
16	chr3:23373000-23373400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr3:23373000-23373800	Enhancers	Pancreas	Pancrea

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links