Variant report

Variant	rs9295100
Chromosome Location	chr6:159871930-159871931
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:159865666..159867894-chr6:159870973..159873736,2	MCF-7	breast:

Extended variants
information (count: 38 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10755568	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10806715	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13197789	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1416607	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1466176	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1965861	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1965862	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1977751	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2341533	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2341623	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4708828	0.93[ASN][1000 genomes]
rs4708829	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4709326	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4709328	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4709330	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4709331	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58558653	0.88[ASN][1000 genomes]
rs6905920	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6912066	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6919053	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73029896	0.86[ASN][1000 genomes]
rs7752883	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7758076	0.93[ASN][1000 genomes]
rs7771199	0.93[ASN][1000 genomes]
rs9295101	0.95[ASN][1000 genomes]
rs9346788	0.92[ASN][1000 genomes]
rs9346789	0.90[ASN][1000 genomes]
rs9347320	0.88[ASN][1000 genomes]
rs9347321	0.88[ASN][1000 genomes]
rs9355727	0.88[ASN][1000 genomes]
rs9364522	0.90[ASN][1000 genomes]
rs9365061	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9365064	0.90[ASN][1000 genomes]
rs9456406	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[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	nsv1030483	chr6:159475679-159910480	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv538490	chr6:159475679-159910480	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	esv2763604	chr6:159509373-159942955	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv1019191	chr6:159555100-160043247	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9295100	DYNLT1	cis	cerebellum	SCAN

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:159867000-159876600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:159871200-159872400	Enhancers	Fetal Muscle Leg	muscle
3	chr6:159871200-159873600	Enhancers	Fetal Stomach	stomach
4	chr6:159871600-159872200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:159871600-159872200	Enhancers	Adipose Nuclei	Adipose
6	chr6:159871600-159872600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:159871600-159873000	Enhancers	Fetal Lung	lung
8	chr6:159871800-159872200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:159871800-159872200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
10	chr6:159871800-159872200	Enhancers	Fetal Muscle Trunk	muscle
11	chr6:159871800-159872200	Enhancers	Placenta	Placenta
12	chr6:159871800-159872400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr6:159871800-159872400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr6:159871800-159872400	Enhancers	Placenta Amnion	Placenta Amnion
15	chr6:159871800-159872400	Enhancers	HSMMtube	muscle
16	chr6:159871800-159872600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr6:159871800-159872600	Enhancers	Osteobl	bone
18	chr6:159871800-159872800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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