Variant report

Variant	rs74156007
Chromosome Location	chr1:210829311-210829312
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11804564	1.00[EUR][1000 genomes]
rs12058991	0.82[AFR][1000 genomes]
rs12064860	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12069077	0.88[AFR][1000 genomes]
rs12086850	1.00[EUR][1000 genomes]
rs12092331	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4297293	1.00[EUR][1000 genomes]
rs57402964	0.82[AFR][1000 genomes]
rs58495788	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74156005	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74156006	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74156008	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74158943	1.00[EUR][1000 genomes]
rs74158948	1.00[EUR][1000 genomes]
rs74158964	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

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	nsv873148	chr1:210665583-210994339	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv522480	chr1:210779936-210848344	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA miRNA target site	n/a	inside rSNPs	diseases
3	esv1825229	chr1:210789477-210854976	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA miRNA target site	n/a	inside rSNPs	diseases
4	nsv873150	chr1:210808270-210893233	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
5	nsv873151	chr1:210818347-210846888	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv873152	chr1:210820285-210854815	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA target site	n/a	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210821400-210837000	Weak transcription	Left Ventricle	heart
2	chr1:210824200-210830000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:210827400-210837200	Weak transcription	Right Ventricle	heart
4	chr1:210827600-210829400	Weak transcription	HSMMtube	muscle
5	chr1:210827600-210830200	Weak transcription	Brain Hippocampus Middle	brain
6	chr1:210827600-210830400	Weak transcription	Brain Anterior Caudate	brain
7	chr1:210827600-210830400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr1:210827600-210830400	Weak transcription	Brain Substantia Nigra	brain
9	chr1:210827600-210830600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr1:210827600-210830600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr1:210827600-210830600	Weak transcription	Fetal Lung	lung
12	chr1:210827600-210831000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr1:210827600-210831200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr1:210827600-210831800	Weak transcription	Stomach Smooth Muscle	stomach
15	chr1:210827600-210836400	Weak transcription	Fetal Heart	heart
16	chr1:210827600-210836800	Weak transcription	Brain Angular Gyrus	brain
17	chr1:210827600-210837000	Weak transcription	Gastric	stomach
18	chr1:210827600-210843400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr1:210827600-210847600	Weak transcription	HSMM	muscle
20	chr1:210828600-210829800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr1:210829000-210829600	Weak transcription	Spleen	Spleen
22	chr1:210829000-210853400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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