Variant report

Variant	rs250490
Chromosome Location	chr5:15975251-15975252
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs168747	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs181833	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs250489	0.85[ASN][1000 genomes]
rs250496	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs250497	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs250498	0.95[ASN][1000 genomes]
rs250500	0.95[ASN][1000 genomes]
rs250503	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs250504	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2599492	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2599503	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs32823	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs32824	0.81[ASN][1000 genomes]
rs32826	0.99[ASN][1000 genomes]
rs32829	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs32830	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4701645	0.84[AMR][1000 genomes]
rs4701646	0.84[AMR][1000 genomes]
rs6859383	0.89[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830216	chr5:15860662-16060420	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv427712	chr5:15883439-16055856	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
3	esv3449880	chr5:15975021-15975296	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:15970400-15981000	Weak transcription	Right Ventricle	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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