Variant report

Variant	rs68024979
Chromosome Location	chr14:85723801-85723802
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12431801	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12432038	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12432305	1.00[ASN][1000 genomes]
rs12433588	1.00[ASN][1000 genomes]
rs12435059	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12435067	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12435945	1.00[ASN][1000 genomes]
rs12436027	1.00[ASN][1000 genomes]
rs12589547	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17120910	0.90[EUR][1000 genomes]
rs4904243	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55808777	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57832147	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66538839	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66793589	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72687566	1.00[ASN][1000 genomes]
rs72689111	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73310242	0.81[AFR][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	esv2422273	chr14:85703149-85767292	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:85717200-85727800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr14:85723600-85724200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr14:85723800-85724000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr14:85723800-85724600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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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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