Variant report

Variant	rs72732520
Chromosome Location	chr5:36584472-36584473
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs67860431	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6865986	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6894941	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6895261	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][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	nsv492319	chr5:36570707-37061019	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv881025	chr5:36575021-36613053	Weak transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
3	nsv830263	chr5:36576504-36755093	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36583800-36584800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr5:36583800-36584800	Enhancers	Brain Angular Gyrus	brain
3	chr5:36583800-36585000	Enhancers	Brain Hippocampus Middle	brain
4	chr5:36583800-36586200	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr5:36584000-36584600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr5:36584000-36584800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:36584000-36584800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
8	chr5:36584000-36584800	Flanking Active TSS	Brain Substantia Nigra	brain
9	chr5:36584000-36584800	Enhancers	Right Atrium	heart
10	chr5:36584000-36585200	Enhancers	Brain Anterior Caudate	brain
11	chr5:36584200-36585600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr5:36584200-36586400	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr5:36584400-36584600	Enhancers	Brain Cingulate Gyrus	brain
14	chr5:36584400-36584800	Active TSS	Adipose Nuclei	Adipose
15	chr5:36584400-36584800	Enhancers	Spleen	Spleen
16	chr5:36584400-36585000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:36584400-36585000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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