Variant report

Variant	rs73585267
Chromosome Location	chr10:4078355-4078356
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs17131942	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17349974	1.00[ASN][1000 genomes]
rs2250230	0.90[EUR][1000 genomes]
rs2765654	0.97[EUR][1000 genomes]
rs73585275	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73585277	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs943020	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051297	chr10:3908706-4277678	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv831772	chr10:4039292-4212218	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1046213	chr10:4059937-4144692	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv540460	chr10:4059937-4144692	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4066400-4081200	Weak transcription	Gastric	stomach
2	chr10:4076000-4078400	Enhancers	Fetal Muscle Leg	muscle
3	chr10:4076600-4081000	Enhancers	Dnd41	blood
4	chr10:4076800-4078400	Enhancers	Fetal Thymus	thymus
5	chr10:4077600-4078400	Enhancers	Primary B cells from cord blood	blood
6	chr10:4077600-4078400	Enhancers	Primary hematopoietic stem cells	blood
7	chr10:4077600-4078400	Enhancers	Placenta Amnion	Placenta Amnion
8	chr10:4077600-4089200	Weak transcription	Ovary	ovary
9	chr10:4077800-4078400	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr10:4077800-4078400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr10:4078000-4078400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr10:4078000-4078600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr10:4078000-4078600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr10:4078000-4083400	Weak transcription	Adipose Nuclei	Adipose

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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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