Variant report

Variant	rs72667934
Chromosome Location	chr1:58563696-58563697
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs6694980	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72667932	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72667936	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs72667941	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72667945	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72667954	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72667988	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015057	chr1:57976993-58793962	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv530017	chr1:58002290-58669736	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv431379	chr1:58224212-58802608	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:58562600-58563800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr1:58562600-58564600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr1:58563400-58564000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr1:58563400-58564200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr1:58563400-58564200	Enhancers	H9 Cell Line	embryonic stem cell
6	chr1:58563400-58564200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr1:58563400-58564200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:58563400-58564200	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr1:58563400-58564800	Enhancers	Primary hematopoietic stem cells	blood
10	chr1:58563600-58564000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr1:58563600-58564200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr1:58563600-58564200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr1:58563600-58564400	Enhancers	iPS-18 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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