Variant report

Variant	rs74089558
Chromosome Location	chr1:72488418-72488419
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12065683	1.00[AMR][1000 genomes]
rs17091927	0.89[AFR][1000 genomes]
rs17092138	1.00[AFR][1000 genomes]
rs17092179	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74086910	1.00[AMR][1000 genomes]
rs74087197	1.00[AMR][1000 genomes]
rs74088180	1.00[AMR][1000 genomes]
rs74089563	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74089577	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817447	chr1:72098815-72558020	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv916783	chr1:72196061-72707953	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1007910	chr1:72247302-72543998	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv428763	chr1:72353556-72499701	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1007073	chr1:72419858-72734657	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv546478	chr1:72442018-72512391	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1006076	chr1:72477436-72700903	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv534996	chr1:72477436-72700903	Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72476200-72488800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr1:72484600-72489600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr1:72484800-72488600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr1:72484800-72488600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr1:72484800-72488600	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr1:72484800-72490200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:72488200-72488600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr1:72488400-72488600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr1:72488400-72488600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr1:72488400-72488600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr1:72488400-72490800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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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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