Variant report

Variant	rs73011528
Chromosome Location	chr3:155174031-155174032
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11928539	0.94[AFR][1000 genomes]
rs16824956	0.91[AFR][1000 genomes]
rs16824961	0.91[AFR][1000 genomes]
rs16824962	0.91[AFR][1000 genomes]
rs16824965	0.94[AFR][1000 genomes]
rs16824986	0.94[AFR][1000 genomes]
rs16824992	0.94[AFR][1000 genomes]
rs57461710	0.94[AFR][1000 genomes]
rs57951243	0.91[AFR][1000 genomes]
rs57985049	0.94[AFR][1000 genomes]
rs73009787	0.91[AFR][1000 genomes]
rs73009792	0.90[AFR][1000 genomes]
rs73009795	0.91[AFR][1000 genomes]
rs73011503	0.91[AFR][1000 genomes]
rs73011509	0.91[AFR][1000 genomes]
rs73011512	0.94[AFR][1000 genomes]
rs73011513	0.94[AFR][1000 genomes]
rs73011515	0.94[AFR][1000 genomes]
rs73011519	0.91[AFR][1000 genomes]
rs73011523	0.87[AFR][1000 genomes]
rs73011525	0.93[AFR][1000 genomes]
rs73011526	0.93[AFR][1000 genomes]
rs73011527	0.93[AFR][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	nsv999994	chr3:154579254-155175303	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv1000753	chr3:154848433-155207022	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv536773	chr3:154848433-155207022	Enhancers Strong transcription Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
4	nsv877679	chr3:155128968-155204939	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155166800-155178800	Weak transcription	Pancreas	Pancrea
2	chr3:155170000-155179000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:155172400-155179400	Weak transcription	Dnd41	blood
4	chr3:155173200-155174600	Weak transcription	Fetal Intestine Small	intestine
5	chr3:155173200-155174800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr3:155173800-155182400	Weak transcription	Gastric	stomach

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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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