Variant report

Variant	rs73408096
Chromosome Location	chr12:119557687-119557688
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs58472164	1.00[AMR][1000 genomes]
rs59156247	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73405980	1.00[AMR][1000 genomes]
rs73405982	1.00[AMR][1000 genomes]
rs73405986	1.00[AMR][1000 genomes]
rs73405988	1.00[AMR][1000 genomes]
rs73408073	1.00[AFR][1000 genomes]
rs73408085	1.00[AFR][1000 genomes]
rs73412021	1.00[AMR][1000 genomes]
rs73412027	1.00[AMR][1000 genomes]
rs73412047	1.00[AMR][1000 genomes]
rs7966496	0.96[AFR][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	nsv1047036	chr12:119477583-119992640	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv455725	chr12:119532430-119558565	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv560395	chr12:119532430-119558565	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119535200-119568800	Weak transcription	Fetal Brain Male	brain
2	chr12:119553600-119567600	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr12:119553800-119558800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr12:119553800-119569000	Weak transcription	Brain Angular Gyrus	brain
5	chr12:119555800-119559000	Strong transcription	Brain Germinal Matrix	brain
6	chr12:119557600-119558000	Weak transcription	Fetal Brain Female	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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