Variant report

Variant	rs73515776
Chromosome Location	chr11:83857092-83857093
allele	C/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:17)

rs_ID	r²[population]
rs1598072	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17146742	1.00[AMR][1000 genomes]
rs17146774	1.00[AMR][1000 genomes]
rs56845215	1.00[AMR][1000 genomes]
rs59497240	1.00[AMR][1000 genomes]
rs60264188	1.00[AMR][1000 genomes]
rs73513723	1.00[AMR][1000 genomes]
rs73513766	1.00[AMR][1000 genomes]
rs73513787	1.00[AMR][1000 genomes]
rs73515710	1.00[AMR][1000 genomes]
rs73515738	1.00[AMR][1000 genomes]
rs73515748	1.00[AMR][1000 genomes]
rs73515779	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73515790	1.00[AMR][1000 genomes]
rs73517704	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73517747	1.00[AMR][1000 genomes]
rs73519723	1.00[AMR][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	nsv1039924	chr11:83662904-83993497	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv541102	chr11:83662904-83993497	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv898029	chr11:83717887-83939591	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1051279	chr11:83818647-83872815	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83846600-83858200	Enhancers	Brain Hippocampus Middle	brain
2	chr11:83853600-83858200	Enhancers	Brain Substantia Nigra	brain
3	chr11:83854800-83858400	Enhancers	Brain Anterior Caudate	brain
4	chr11:83855200-83857800	Enhancers	Brain Angular Gyrus	brain
5	chr11:83855400-83858400	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr11:83856000-83857200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr11:83856600-83857200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr11:83856800-83857200	Enhancers	Fetal Kidney	kidney
9	chr11:83856800-83857800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr11:83856800-83858200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr11:83857000-83858000	Weak transcription	Brain Cingulate Gyrus	brain
12	chr11:83857000-83858200	Enhancers	Fetal Heart	heart

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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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