Variant report

Variant	rs72649211
Chromosome Location	chr8:64515793-64515794
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs72665543	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	nsv831343	chr8:64436268-64642328	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64509800-64516000	Weak transcription	Brain Germinal Matrix	brain
2	chr8:64514800-64517600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr8:64514800-64517800	Weak transcription	Fetal Brain Female	brain
4	chr8:64515000-64517600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr8:64515000-64517800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:64515200-64517600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr8:64515200-64517800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr8:64515600-64519800	Enhancers	Fetal Brain Male	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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