Variant report

Variant	rs1698250
Chromosome Location	chr14:84356833-84356834
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:14)

rs_ID	r²[population]
rs10148908	0.93[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs11159614	0.98[ASN][1000 genomes]
rs11159616	1.00[JPT][hapmap]
rs12587946	0.92[ASN][1000 genomes]
rs12587963	0.92[ASN][1000 genomes]
rs1619837	0.84[ASN][1000 genomes]
rs1698247	0.99[ASN][1000 genomes]
rs1698249	0.96[AFR][1000 genomes]
rs1705652	0.92[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs1705660	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17119257	0.94[ASN][1000 genomes]
rs1756299	0.84[ASN][1000 genomes]
rs4899843	0.82[ASN][1000 genomes]
rs4899844	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431019	chr14:84303525-84365447	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv902159	chr14:84336944-84447356	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 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	chr14:84354200-84359400	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr14:84354200-84359600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr14:84354400-84362600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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