Variant report

Variant	rs2192420
Chromosome Location	chr14:78862719-78862720
allele	A/G
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]
rs12887245	0.90[CHB][hapmap]
rs17107429	1.00[CEU][hapmap]
rs17107436	0.88[CEU][hapmap]
rs17107446	0.88[CEU][hapmap]
rs17107482	1.00[CEU][hapmap];0.95[CHB][hapmap];0.92[CHD][hapmap];0.80[JPT][hapmap];1.00[TSI][hapmap]
rs214026	0.85[CHB][hapmap]
rs214027	0.85[CHB][hapmap]
rs214028	0.88[CEU][hapmap]
rs214029	0.88[CEU][hapmap]
rs214030	0.88[CEU][hapmap]
rs214031	0.88[CEU][hapmap]
rs2215835	0.88[CEU][hapmap]
rs2215836	0.88[CEU][hapmap]
rs2366155	0.81[CHB][hapmap]
rs7155022	0.90[CHB][hapmap];0.87[GIH][hapmap]

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	nsv832837	chr14:78766805-78946526	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78860600-78864600	Weak transcription	Brain Germinal Matrix	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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