Variant report

Variant	rs524684
Chromosome Location	chr1:175846463-175846464
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10913091	0.82[EUR][1000 genomes]
rs12117735	0.83[EUR][1000 genomes]
rs12118970	0.83[EUR][1000 genomes]
rs1361521	0.83[EUR][1000 genomes]
rs16849285	0.83[EUR][1000 genomes]
rs16849286	0.83[EUR][1000 genomes]
rs478276	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs500894	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72711130	0.82[EUR][1000 genomes]
rs72711137	0.83[EUR][1000 genomes]
rs7517760	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33328	chr1:175446583-175910001	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv872560	chr1:175648631-175869554	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv522255	chr1:175827683-175849898	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:175835600-175848200	Weak transcription	Aorta	Aorta
2	chr1:175838800-175847400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr1:175841600-175846800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr1:175842000-175846800	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr1:175842400-175848600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:175843000-175855000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:175843200-175846800	Weak transcription	Brain Substantia Nigra	brain
8	chr1:175843400-175846800	Weak transcription	Brain Anterior Caudate	brain
9	chr1:175844800-175847600	Enhancers	Fetal Lung	lung
10	chr1:175845400-175846600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:175845600-175848200	Enhancers	Adipose Nuclei	Adipose
12	chr1:175845800-175850400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr1:175846000-175847600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:175846200-175848200	Enhancers	Brain Cingulate Gyrus	brain
15	chr1:175846200-175848600	Enhancers	Brain Germinal Matrix	brain
16	chr1:175846400-175848200	Enhancers	Brain Hippocampus Middle	brain
17	chr1:175846400-175848600	Enhancers	Brain Angular Gyrus	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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