Variant report

Variant	rs7524732
Chromosome Location	chr1:193594794-193594795
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12025400	0.85[EUR][1000 genomes]
rs12064935	0.85[EUR][1000 genomes]
rs12073207	0.81[EUR][1000 genomes]
rs12082580	0.82[EUR][1000 genomes]
rs12084728	0.85[EUR][1000 genomes]
rs12086172	0.95[TSI][hapmap];0.85[EUR][1000 genomes]
rs1339307	0.85[EUR][1000 genomes]
rs1416601	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1578120	0.85[EUR][1000 genomes]
rs16835629	0.85[EUR][1000 genomes]
rs17304644	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap]
rs72728904	0.85[EUR][1000 genomes]
rs72744046	0.85[EUR][1000 genomes]
rs72744048	0.85[EUR][1000 genomes]
rs72744061	0.82[EUR][1000 genomes]
rs72744063	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72744067	0.85[EUR][1000 genomes]
rs72744069	0.84[EUR][1000 genomes]
rs9628684	0.84[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	nsv832170	chr1:193426455-193596182	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv1008266	chr1:193550185-194481053	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr1:193586200-193603200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr1:193589400-193596600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:193594400-193594800	Enhancers	Liver	Liver
4	chr1:193594600-193595000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:193594600-193595800	Weak transcription	Fetal Muscle Leg	muscle

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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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