Variant report

Variant	rs34108484
Chromosome Location	chr4:99691805-99691806
allele	C/T
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]
rs1406034	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1808953	1.00[ASN][1000 genomes]
rs2120376	1.00[ASN][1000 genomes]
rs2178126	0.93[AMR][1000 genomes]
rs2866024	0.80[AFR][1000 genomes]
rs2866025	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2866027	0.93[AMR][1000 genomes]
rs34139935	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34417635	0.93[AMR][1000 genomes]
rs35019282	1.00[ASN][1000 genomes]
rs35070786	1.00[ASN][1000 genomes]
rs35197075	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35248449	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35966034	1.00[ASN][1000 genomes]
rs62325490	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6822967	1.00[ASN][1000 genomes]
rs920806	1.00[ASN][1000 genomes]
rs968054	1.00[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	nsv1009017	chr4:99669441-100406394	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99691600-99692000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
2	chr4:99691600-99692400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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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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