Variant report

Variant	rs72937905
Chromosome Location	chr3:110815915-110815916
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10511291	0.82[EUR][1000 genomes]
rs1351049	0.88[ASN][1000 genomes]
rs1382077	0.88[ASN][1000 genomes]
rs1477846	0.96[ASN][1000 genomes]
rs1477848	0.96[ASN][1000 genomes]
rs1477850	0.88[ASN][1000 genomes]
rs16857350	0.82[EUR][1000 genomes]
rs16857536	0.82[EUR][1000 genomes]
rs16857689	0.88[ASN][1000 genomes]
rs2126714	1.00[ASN][1000 genomes]
rs2399376	0.88[ASN][1000 genomes]
rs57043424	0.92[ASN][1000 genomes]
rs58184851	0.88[ASN][1000 genomes]
rs60037602	0.82[EUR][1000 genomes]
rs60585479	0.92[ASN][1000 genomes]
rs66624862	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72934030	0.82[EUR][1000 genomes]
rs72934034	0.82[EUR][1000 genomes]
rs72934100	0.82[EUR][1000 genomes]
rs72935934	0.82[EUR][1000 genomes]
rs72935952	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72935959	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72935966	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72935968	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72935975	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72935989	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72935999	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72937910	0.96[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs72937915	0.88[ASN][1000 genomes]
rs72937922	0.88[ASN][1000 genomes]
rs72937952	0.92[ASN][1000 genomes]
rs72937960	0.92[ASN][1000 genomes]
rs72937968	0.92[ASN][1000 genomes]
rs72937972	0.92[ASN][1000 genomes]
rs72948795	0.82[EUR][1000 genomes]
rs72948800	0.82[EUR][1000 genomes]
rs7433877	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7648752	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs873132	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs873133	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9288918	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9288919	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9853370	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9882945	0.88[ASN][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	nsv1003106	chr3:110264476-111105943	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv460821	chr3:110637471-111501097	Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv591275	chr3:110637471-111501097	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	esv1850918	chr3:110685181-110889974	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:110799800-110820600	Weak transcription	A549	lung
2	chr3:110800200-110817200	Weak transcription	Gastric	stomach
3	chr3:110802000-110822600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr3:110804000-110817200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr3:110805000-110833600	Weak transcription	NHDF-Ad	bronchial
6	chr3:110807200-110822600	Weak transcription	Fetal Lung	lung
7	chr3:110808600-110817200	Weak transcription	Small Intestine	intestine
8	chr3:110810400-110816400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr3:110813000-110816200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
10	chr3:110813200-110816000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
11	chr3:110813400-110816000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
12	chr3:110813800-110817200	Weak transcription	Colon Smooth Muscle	Colon
13	chr3:110813800-110822600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr3:110814000-110816800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
15	chr3:110814200-110817200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr3:110814400-110816000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr3:110814600-110816000	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr3:110815200-110816000	ZNF genes & repeats	Fetal Stomach	stomach
19	chr3:110815200-110817200	Weak transcription	Dnd41	blood
20	chr3:110815200-110817600	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr3:110815400-110816000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr3:110815400-110816000	Enhancers	Ovary	ovary
23	chr3:110815800-110816000	Enhancers	Left Ventricle	heart

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