Variant report

Variant	rs72872781
Chromosome Location	chr3:60646019-60646020
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs60903409	0.87[AFR][1000 genomes]
rs61076572	0.87[AFR][1000 genomes]
rs72872707	0.87[AFR][1000 genomes]
rs72872716	0.87[AFR][1000 genomes]
rs72872718	0.87[AFR][1000 genomes]
rs72872723	0.87[AFR][1000 genomes]
rs72872725	0.87[AFR][1000 genomes]
rs72872728	0.87[AFR][1000 genomes]
rs72872733	0.87[AFR][1000 genomes]
rs72872735	0.87[AFR][1000 genomes]
rs72872756	0.87[AFR][1000 genomes]
rs72872760	0.87[AFR][1000 genomes]
rs72872800	1.00[AFR][1000 genomes]
rs72874926	1.00[AFR][1000 genomes]
rs72874953	0.95[AFR][1000 genomes]
rs72874956	0.95[AFR][1000 genomes]
rs72887661	0.87[AFR][1000 genomes]
rs72887684	0.91[AFR][1000 genomes]
rs72889612	0.91[AFR][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	nsv529602	chr3:60088353-60830769	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv998815	chr3:60495872-60830769	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv999828	chr3:60537384-60785274	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr3:60642600-60655000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:60645000-60646200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr3:60645600-60646200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:60645600-60646200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr3:60645600-60646200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:60645600-60646200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr3:60645600-60646200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr3:60645600-60646400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr3:60645800-60646200	Enhancers	H9 Cell Line	embryonic stem cell
10	chr3:60645800-60646400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:60646000-60646200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr3:60646000-60646200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr3:60646000-60646400	Enhancers	Primary neutrophils fromperipheralblood	blood

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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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