Variant report

Variant	rs74092608
Chromosome Location	chr1:77866761-77866762
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]
rs56099019	0.84[AFR][1000 genomes]
rs59272007	1.00[AMR][1000 genomes]
rs59814571	1.00[AMR][1000 genomes]
rs74090490	0.92[AFR][1000 genomes]
rs74090495	0.92[AFR][1000 genomes]
rs74090498	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74090606	1.00[AMR][1000 genomes]
rs74090629	1.00[AMR][1000 genomes]
rs74090656	1.00[AMR][1000 genomes]
rs74092605	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74092606	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74092611	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74092612	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74092614	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74092615	0.85[AFR][1000 genomes];1.00[AMR][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	nsv1005183	chr1:77728990-77949309	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv535010	chr1:77728990-77949309	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv932557	chr1:77730247-77958687	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1003714	chr1:77756861-77949309	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv470719	chr1:77774413-78269207	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv546591	chr1:77774413-78269207	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77845200-77878000	Weak transcription	Primary T cells from cord blood	blood
2	chr1:77845200-77878400	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr1:77861600-77871800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:77863200-77871800	Weak transcription	Aorta	Aorta
5	chr1:77864000-77867400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
6	chr1:77864200-77871200	Weak transcription	HSMMtube	muscle
7	chr1:77864400-77870600	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr1:77865000-77867800	Enhancers	NHDF-Ad	bronchial
9	chr1:77865200-77867200	Enhancers	Osteobl	bone
10	chr1:77865600-77867000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr1:77865600-77877200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr1:77865800-77867200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:77865800-77871800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:77866000-77866800	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr1:77866000-77867200	Weak transcription	Brain Angular Gyrus	brain
16	chr1:77866000-77867200	Weak transcription	Brain Anterior Caudate	brain
17	chr1:77866000-77867400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:77866000-77867800	Enhancers	Brain Cingulate Gyrus	brain
19	chr1:77866000-77871000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr1:77866200-77871000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr1:77866200-77871000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:77866400-77867000	Weak transcription	Brain Substantia Nigra	brain
23	chr1:77866600-77870600	Weak transcription	Brain Hippocampus Middle	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links