Variant report

Variant	rs9995267
Chromosome Location	chr4:62126446-62126447
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10446785	0.80[ASN][1000 genomes]
rs10446793	0.80[ASN][1000 genomes]
rs1505662	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1505674	0.81[ASN][1000 genomes]
rs1505675	0.81[ASN][1000 genomes]
rs1505676	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1505677	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2202499	0.84[ASN][1000 genomes]
rs2342456	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3860621	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3860622	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7435420	0.84[ASN][1000 genomes]
rs7683030	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[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	nsv879075	chr4:62124531-62354791	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:62111400-62129400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:62116000-62127000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr4:62119800-62127400	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr4:62120600-62126600	Weak transcription	Brain Anterior Caudate	brain
5	chr4:62122000-62128200	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr4:62124400-62127000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr4:62124400-62127800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr4:62124600-62129200	Weak transcription	Fetal Heart	heart
9	chr4:62125400-62126600	Weak transcription	Brain Angular Gyrus	brain
10	chr4:62125400-62127200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr4:62126400-62128000	Enhancers	Brain Substantia Nigra	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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