Variant report

Variant	rs1977501
Chromosome Location	chr10:90918714-90918715
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10430718	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10509567	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10887920	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10887921	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10887922	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10887923	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10887925	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10887926	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10887927	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10887928	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10887929	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10887932	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11203006	0.93[ASN][1000 genomes]
rs11203009	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11203011	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11203014	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11203017	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11203018	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11203024	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11203025	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11203030	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11203031	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11203032	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11203033	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12217507	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12219735	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17117088	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17117124	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17117126	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2154255	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2211599	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2863216	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2902445	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3802658	0.82[EUR][1000 genomes]
rs3923282	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4078488	0.86[AMR][1000 genomes]
rs4294494	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4399251	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4417181	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4511206	0.86[AMR][1000 genomes]
rs4617498	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4933494	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4934454	0.94[ASN][1000 genomes]
rs61853072	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6586173	0.89[ASN][1000 genomes]
rs7076185	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7098394	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7477966	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7896174	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9651424	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9651495	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][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	nsv1042848	chr10:90466032-91318474	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv540741	chr10:90466032-91318474	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv831944	chr10:90822654-90967018	Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
4	esv2758235	chr10:90835064-91017486	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2759775	chr10:90835064-91017486	Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv895881	chr10:90842431-90940003	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1041964	chr10:90861380-91378356	Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90913400-90923000	Weak transcription	NHEK	skin
2	chr10:90913600-90923000	Weak transcription	HMEC	breast
3	chr10:90913800-90918800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr10:90916000-90921200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr10:90916400-90919600	Enhancers	NHDF-Ad	bronchial
6	chr10:90917200-90920400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr10:90917600-90920200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr10:90917800-90920400	Enhancers	Osteobl	bone
9	chr10:90918200-90918800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr10:90918200-90919000	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr10:90918200-90919600	Enhancers	Adipose Nuclei	Adipose
12	chr10:90918400-90918800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr10:90918400-90918800	Enhancers	HSMM	muscle
14	chr10:90918400-90919000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr10:90918400-90919400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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