Variant report

Variant	rs73103072
Chromosome Location	chr1:217279147-217279148
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12070441	1.00[AMR][1000 genomes]
rs73103054	1.00[AMR][1000 genomes]
rs73103075	1.00[AMR][1000 genomes]
rs73103078	1.00[AMR][1000 genomes]
rs73103086	1.00[AMR][1000 genomes]
rs73103102	1.00[AMR][1000 genomes]
rs73104927	1.00[AMR][1000 genomes]
rs73104933	1.00[AMR][1000 genomes]
rs73104936	1.00[AMR][1000 genomes]
rs73107043	1.00[AMR][1000 genomes]
rs73107053	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428610	chr1:217143317-217307243	Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:217278800-217279400	Enhancers	Pancreas	Pancrea
2	chr1:217278800-217279800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr1:217279000-217280200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:217279000-217280400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	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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