Variant report

Variant	rs73143135
Chromosome Location	chr3:24684399-24684400
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12635920	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12639068	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17014996	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55707778	0.94[ASN][1000 genomes]
rs56400902	0.85[ASN][1000 genomes]
rs56898952	0.84[ASN][1000 genomes]
rs60800624	0.93[ASN][1000 genomes]
rs6550880	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6550881	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs66815650	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72619931	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7610415	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7631804	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7645619	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7651543	0.86[AMR][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	esv2757862	chr3:24652513-24942926	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2759135	chr3:24652513-24942926	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr3:24683400-24684400	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr3:24683600-24694800	Weak transcription	Fetal Intestine Small	intestine
3	chr3:24684000-24684400	Enhancers	H1 Cell Line	embryonic stem cell

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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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