Variant report

Variant	rs72780637
Chromosome Location	chr10:45421903-45421904
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11239287	0.93[ASN][1000 genomes]
rs11595747	0.93[ASN][1000 genomes]
rs11598392	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1332628	0.93[ASN][1000 genomes]
rs17417060	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs17515726	0.96[ASN][1000 genomes]
rs72778837	1.00[AFR][1000 genomes]
rs72778871	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs949607	0.93[ASN][1000 genomes]
rs952956	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831845	chr10:45300268-45460395	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv831846	chr10:45322236-45556370	Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv466909	chr10:45408011-45446791	Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv550714	chr10:45408011-45446791	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	esv3374788	chr10:45419346-45423644	Genic enhancers Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv818757	chr10:45420076-45431321	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45407800-45422800	Weak transcription	Ovary	ovary
2	chr10:45410200-45430400	Weak transcription	Gastric	stomach
3	chr10:45413400-45428200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr10:45417000-45434000	Weak transcription	Fetal Brain Female	brain
5	chr10:45417800-45422400	Weak transcription	Duodenum Mucosa	Duodenum
6	chr10:45418800-45424800	Weak transcription	Colonic Mucosa	Colon
7	chr10:45420200-45422200	Enhancers	HepG2	liver
8	chr10:45420400-45428000	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr10:45420400-45428200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr10:45420800-45422800	Weak transcription	Fetal Thymus	thymus
11	chr10:45421000-45422400	Weak transcription	Pancreas	Pancrea
12	chr10:45421000-45422800	Weak transcription	Fetal Muscle Trunk	muscle
13	chr10:45421000-45423200	Weak transcription	Lung	lung
14	chr10:45421000-45427800	Weak transcription	Right Ventricle	heart
15	chr10:45421200-45422200	Weak transcription	HSMMtube	muscle
16	chr10:45421200-45422400	Weak transcription	Fetal Muscle Leg	muscle
17	chr10:45421600-45428000	Weak transcription	Fetal Heart	heart
18	chr10:45421800-45422400	Weak transcription	Spleen	Spleen
19	chr10:45421800-45425200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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