Variant report

Variant	rs73311568
Chromosome Location	chr5:144998770-144998771
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:17)

rs_ID	r²[population]
rs10036664	1.00[EUR][1000 genomes]
rs10077242	1.00[EUR][1000 genomes]
rs13354398	1.00[EUR][1000 genomes]
rs13356403	1.00[EUR][1000 genomes]
rs34207413	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4345360	1.00[EUR][1000 genomes]
rs55695946	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57017606	1.00[EUR][1000 genomes]
rs57301309	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57342170	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57791987	1.00[EUR][1000 genomes]
rs58878643	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60380240	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73311522	1.00[EUR][1000 genomes]
rs73311531	1.00[EUR][1000 genomes]
rs73311570	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73311572	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv883004	chr5:144945649-145068001	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv883005	chr5:144945649-145107586	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region lncRNA	2 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	chr5:144997400-145003200	Weak transcription	Ovary	ovary
2	chr5:144998200-144999200	ZNF genes & repeats	Fetal Stomach	stomach
3	chr5:144998600-145003200	Weak transcription	H1 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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