Variant report

Variant	rs10807322
Chromosome Location	chr6:45542617-45542618
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RUNX2-1	chr6:45540498-45543034	XLOC_005302

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10485421	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10948241	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11753640	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12201995	0.89[ASN][1000 genomes]
rs12204264	0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12664797	0.86[ASN][1000 genomes]
rs13200687	1.00[JPT][hapmap]
rs1928532	0.85[EUR][1000 genomes]
rs2280225	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2280226	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2280227	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2280228	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2280229	0.91[ASN][1000 genomes]
rs2280230	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs34528484	0.81[ASN][1000 genomes]
rs35611098	0.89[ASN][1000 genomes]
rs3763191	0.86[ASN][1000 genomes]
rs68057028	0.89[ASN][1000 genomes]
rs6913882	0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs6914235	0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs6937759	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6938170	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6938214	0.89[ASN][1000 genomes]
rs6938450	0.94[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6938843	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6938991	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7752324	0.84[ASN][1000 genomes]
rs7754569	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7758107	0.84[ASN][1000 genomes]
rs7758317	0.84[ASN][1000 genomes]
rs9296461	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9463102	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs9463103	0.81[ASN][1000 genomes]
rs9472507	0.91[ASN][1000 genomes]
rs9472508	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028393	chr6:44875558-45822335	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv538211	chr6:44875558-45822335	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv427755	chr6:45474631-45627025	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv532024	chr6:45475088-45982640	Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv603009	chr6:45530471-45543530	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv462940	chr6:45532214-45545975	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv603010	chr6:45532214-45545975	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45537400-45544800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:45537400-45559000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:45537600-45544400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr6:45537600-45544600	Weak transcription	Left Ventricle	heart
5	chr6:45537600-45544600	Weak transcription	Lung	lung
6	chr6:45537600-45545200	Weak transcription	NH-A	brain
7	chr6:45537600-45546000	Weak transcription	Right Atrium	heart
8	chr6:45537800-45544600	Weak transcription	Brain Hippocampus Middle	brain
9	chr6:45538800-45544800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:45539400-45544400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:45540600-45542800	Enhancers	HepG2	liver
12	chr6:45540600-45543000	Enhancers	Esophagus	oesophagus
13	chr6:45541000-45543000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr6:45542000-45543000	Enhancers	Dnd41	blood
15	chr6:45542000-45543400	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr6:45542200-45542800	Enhancers	HMEC	breast
17	chr6:45542400-45542800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:45542600-45542800	Enhancers	Primary hematopoietic stem cells	blood
19	chr6:45542600-45543000	Enhancers	Fetal Thymus	thymus
20	chr6:45542600-45543200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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