Variant report

Variant	rs73437648
Chromosome Location	chr7:68959257-68959258
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10256483	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10257731	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10265122	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10281633	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10950189	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10950190	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11771876	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12155091	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12530810	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12531644	0.94[EUR][1000 genomes]
rs12538348	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12698802	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12698803	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12698804	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13243683	0.83[AFR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13246613	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1541427	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17137493	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1981585	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1981586	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2108046	0.80[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs2865169	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28758447	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35245526	0.89[EUR][1000 genomes]
rs41862	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs41863	0.80[EUR][1000 genomes]
rs41865	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4268006	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55714924	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56854903	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6460521	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6944163	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6946622	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6975413	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6979168	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7785268	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7810187	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023885	chr7:68894896-69158290	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv538915	chr7:68894896-69158290	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv916011	chr7:68942155-69330800	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv5782	chr7:68946883-68991904	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:68957800-68961200	Enhancers	Primary B cells from cord blood	blood
2	chr7:68958200-68960200	Enhancers	Primary B cells from peripheral blood	blood
3	chr7:68958400-68959400	Enhancers	Fetal Thymus	thymus
4	chr7:68958400-68959400	Enhancers	Dnd41	blood
5	chr7:68958400-68960000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr7:68958400-68960200	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr7:68958400-68960200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr7:68958400-68960400	Enhancers	Primary hematopoietic stem cells	blood
9	chr7:68958600-68960000	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr7:68959000-68960000	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr7:68959200-68959400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:68959200-68961000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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