Variant report

Variant	rs73311572
Chromosome Location	chr5:144999775-144999776
allele	A/G
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	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57017606	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs57301309	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57342170	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57791987	1.00[EUR][1000 genomes]
rs58878643	0.95[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]
rs73311568	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73311570	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:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:144997400-145003200	Weak transcription	Ovary	ovary
2	chr5:144998600-145003200	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr5:144998800-145000400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr5:144999000-145000400	Enhancers	NHLF	lung
5	chr5:144999200-145000200	Weak transcription	Fetal Stomach	stomach

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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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