Variant report

Variant	rs73236515
Chromosome Location	chr3:140936434-140936435
allele	C/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:13)

rs_ID	r²[population]
rs1871278	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2291040	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55655840	1.00[EUR][1000 genomes]
rs55839795	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55877951	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56293064	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73232931	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73232934	0.92[EUR][1000 genomes]
rs73236512	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73236514	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73236516	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73236517	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73236521	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140931800-140941200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr3:140934400-140938400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:140935000-140937000	Enhancers	HepG2	liver
4	chr3:140935800-140937800	Enhancers	Fetal Intestine Large	intestine
5	chr3:140935800-140938800	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr3:140936000-140936600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr3:140936000-140937400	Enhancers	Psoas Muscle	Psoas
8	chr3:140936000-140937600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr3:140936000-140937800	Enhancers	Primary B cells from cord blood	blood
10	chr3:140936200-140936600	Enhancers	Liver	Liver
11	chr3:140936200-140937800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr3:140936400-140936600	Enhancers	Left Ventricle	heart
13	chr3:140936400-140936800	Enhancers	Duodenum Mucosa	Duodenum
14	chr3:140936400-140937600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr3:140936400-140940000	Enhancers	Fetal Heart	heart

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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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