Variant report

Variant	rs62180373
Chromosome Location	chr2:180621268-180621269
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs17774088	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2171190	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4390734	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4556941	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4558554	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62180369	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62180372	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62180377	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62180379	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62180380	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62180381	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62180382	0.94[EUR][1000 genomes]
rs62180383	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62180384	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62180385	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62180386	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62180387	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62180388	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62180389	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62180390	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62180391	0.94[EUR][1000 genomes]
rs62180393	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62180408	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62181522	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62181527	1.00[AMR][1000 genomes];0.98[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	nsv1002305	chr2:180568558-180812846	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 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	chr2:180621200-180624200	ZNF genes & repeats	H1 Derived Neuronal Progenitor 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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