Variant report

Variant	rs1017415
Chromosome Location	chr18:24363110-24363111
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1020477	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1823366	0.81[AMR][1000 genomes]
rs1865540	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4800269	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs55841767	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs8087166	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs8089326	0.85[AMR][1000 genomes];0.82[EUR][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:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:24360200-24363200	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr18:24360200-24364600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr18:24361000-24363800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr18:24361200-24364800	Weak transcription	Brain Cingulate Gyrus	brain
5	chr18:24362000-24364800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr18:24362200-24363600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr18:24362400-24365800	Weak transcription	H1 BMP4 Derived Mesendoderm 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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