Variant report

Variant	rs7591725
Chromosome Location	chr2:7392102-7392103
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12613310	0.82[EUR][1000 genomes]
rs1525496	0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2140855	0.94[ASN][1000 genomes]
rs4668532	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4669168	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4669171	0.90[EUR][1000 genomes]
rs6431869	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72277251	0.83[EUR][1000 genomes]
rs7576780	0.82[ASN][1000 genomes]
rs7595799	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs876998	0.81[AMR][1000 genomes];0.92[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	nsv915888	chr2:7197783-7461967	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv833337	chr2:7337273-7521146	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr2:7383200-7399800	Weak transcription	Spleen	Spleen
2	chr2:7389600-7402600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr2:7391000-7395400	Weak transcription	Fetal Brain Female	brain

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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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