Variant report

Variant	rs1786651
Chromosome Location	chr18:24371110-24371111
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1435420	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1435421	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs473026	0.86[ASN][1000 genomes]
rs487455	0.86[ASN][1000 genomes]
rs491718	0.95[EUR][1000 genomes]
rs495970	0.89[ASN][1000 genomes]
rs516788	0.84[ASN][1000 genomes]
rs536381	0.91[ASN][1000 genomes]
rs536522	0.86[ASN][1000 genomes]
rs583692	0.91[ASN][1000 genomes]
rs603731	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs606771	0.80[ASN][1000 genomes]
rs621765	0.91[ASN][1000 genomes]
rs647839	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8089978	0.89[ASN][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	esv2761995	chr18:24214286-24502570	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:24364800-24371600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr18:24365400-24372600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr18:24369000-24371800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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