Variant report

Variant	rs72651781
Chromosome Location	chr10:134775-134776
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11253286	1.00[ASN][1000 genomes]
rs2379069	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9286070	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9419460	1.00[ASN][1000 genomes]
rs9419473	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9419475	0.82[EUR][1000 genomes]
rs9419539	1.00[ASN][1000 genomes]
rs9419556	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9419557	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9419560	0.82[EUR][1000 genomes]
rs9419561	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9419562	0.82[EUR][1000 genomes]
rs9419564	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531919	chr10:60001-668649	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1040332	chr10:72797-244561	Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1044775	chr10:72797-250662	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1047868	chr10:72797-259003	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv1048232	chr10:72797-274675	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:132000-135400	Enhancers	Stomach Mucosa	stomach
2	chr10:132800-135000	Enhancers	Fetal Intestine Small	intestine
3	chr10:133000-135000	Enhancers	Pancreas	Pancrea
4	chr10:133200-135000	Enhancers	Placenta Amnion	Placenta Amnion
5	chr10:133600-135800	Enhancers	Placenta	Placenta
6	chr10:133800-135200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr10:133800-135400	Weak transcription	NHEK	skin
8	chr10:134000-136200	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr10:134400-136800	Enhancers	HepG2	liver
10	chr10:134600-137400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr10:134600-137400	Weak transcription	Gastric	stomach
12	chr10:134600-137800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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

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