Variant report

Variant	rs73962037
Chromosome Location	chr2:145336863-145336864
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:145336611..145338809-chr2:146171672..146173388,2	K562	blood:
2	chr2:145264650..145290093-chr2:145328018..145347614,89	K562	blood:
3	chr2:145335245..145338135-chr2:145376497..145379162,2	K562	blood:
4	chr2:145260780..145283431-chr2:145335698..145347428,65	K562	blood:
5	chr2:145325314..145328717-chr2:145336202..145340308,3	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP15-5	chr2:145336776-145337001	ENSG00000232606

No data

No data

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1158330	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1159677	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1256912	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1256915	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4662228	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56046235	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57628678	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6430062	1.00[AMR][1000 genomes]
rs73962030	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73962031	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73962032	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73962033	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73962036	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73962038	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73962039	0.81[AFR][1000 genomes]
rs73962041	0.81[AFR][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	nsv1067624	chr2:144657717-145425705	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv531413	chr2:144657717-145425705	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv916172	chr2:144970681-145425713	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv948474	chr2:145035890-145436665	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
5	nsv1002563	chr2:145182201-145863253	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv535957	chr2:145182201-145863253	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv531662	chr2:145219415-145422833	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	nsv529501	chr2:145257682-145485605	Active TSS Enhancers Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 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	chr2:145327600-145338000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr2:145331000-145337000	Weak transcription	K562	blood
3	chr2:145331600-145337800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:145335000-145337200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr2:145335000-145338000	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr2:145336200-145337000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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