Variant report

Variant	rs73156402
Chromosome Location	chr3:93831777-93831778
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10454213	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13070047	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13071953	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13074114	0.89[EUR][1000 genomes]
rs13092355	0.88[EUR][1000 genomes]
rs13100168	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17855824	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs33944211	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34029886	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34333966	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34424617	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34533857	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34703980	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35001908	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35674819	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35772508	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35929728	0.92[EUR][1000 genomes]
rs35937148	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs36049016	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs36075561	0.83[ASN][1000 genomes]
rs6790067	0.81[AMR][1000 genomes]
rs68145886	0.89[EUR][1000 genomes]
rs71326806	0.84[EUR][1000 genomes]
rs73156337	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73156339	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73156384	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73159590	0.91[ASN][1000 genomes]
rs73159600	0.87[ASN][1000 genomes]
rs73159602	0.87[ASN][1000 genomes]
rs7609644	0.89[EUR][1000 genomes]
rs7615840	0.89[EUR][1000 genomes]
rs7616142	0.83[EUR][1000 genomes]
rs7645522	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8178592	0.89[EUR][1000 genomes]
rs8178615	0.83[EUR][1000 genomes]
rs8178635	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869241	chr3:93527675-94504491	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv998173	chr3:93575084-94427403	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv536644	chr3:93575084-94427403	Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv1008711	chr3:93575284-94427264	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv536646	chr3:93575284-94427264	Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv491829	chr3:93575285-94427263	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	esv1795060	chr3:93602038-93848525	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	n/a
8	esv1791740	chr3:93602927-93849247	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	n/a
9	esv2755326	chr3:93605126-93882750	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	n/a
10	nsv1013107	chr3:93654100-94102212	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
11	nsv536648	chr3:93654100-94102212	Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
12	nsv1004176	chr3:93654100-94502551	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
13	nsv877162	chr3:93779664-94278078	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
14	nsv877163	chr3:93795972-94047775	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:93782800-93848200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:93782800-93849400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr3:93783200-93851600	Weak transcription	HMEC	breast
4	chr3:93783400-93833000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr3:93783600-93837800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr3:93785600-93834400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr3:93786200-93834600	Weak transcription	Brain Substantia Nigra	brain
8	chr3:93786800-93849800	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr3:93791400-93841200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr3:93792200-93833200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr3:93795600-93847000	Weak transcription	Osteobl	bone
12	chr3:93796000-93857800	Weak transcription	Fetal Brain Male	brain
13	chr3:93799000-93851600	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr3:93800200-93851000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr3:93802400-93849600	Weak transcription	Stomach Mucosa	stomach
16	chr3:93802600-93851800	Weak transcription	Small Intestine	intestine
17	chr3:93803400-93835800	Weak transcription	Psoas Muscle	Psoas
18	chr3:93804400-93834600	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr3:93804800-93833000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr3:93806400-93834800	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr3:93808400-93849600	Weak transcription	Fetal Heart	heart
22	chr3:93811400-93832800	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr3:93812400-93852200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr3:93814600-93845200	Weak transcription	Esophagus	oesophagus
25	chr3:93814600-93847000	Weak transcription	Spleen	Spleen
26	chr3:93814600-93849400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr3:93814600-93849400	Weak transcription	Right Ventricle	heart
28	chr3:93814600-93849600	Weak transcription	Brain Hippocampus Middle	brain
29	chr3:93814600-93849800	Weak transcription	Colonic Mucosa	Colon
30	chr3:93814800-93845200	Weak transcription	Gastric	stomach
31	chr3:93814800-93857800	Weak transcription	Pancreas	Pancrea
32	chr3:93815400-93834200	Weak transcription	Brain Anterior Caudate	brain
33	chr3:93815600-93848400	Weak transcription	Placenta	Placenta
34	chr3:93815800-93832800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr3:93816600-93834600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr3:93817200-93844800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr3:93817400-93833000	Weak transcription	NHDF-Ad	bronchial
38	chr3:93817400-93849600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr3:93817600-93837200	Weak transcription	Colon Smooth Muscle	Colon
40	chr3:93817600-93847000	Weak transcription	HepG2	liver
41	chr3:93817600-93848000	Weak transcription	NH-A	brain
42	chr3:93817800-93843000	Weak transcription	Rectal Smooth Muscle	rectum
43	chr3:93817800-93846000	Weak transcription	Brain Angular Gyrus	brain
44	chr3:93817800-93848000	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr3:93818000-93850200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr3:93818600-93843200	Weak transcription	Aorta	Aorta
47	chr3:93818600-93847000	Weak transcription	Lung	lung
48	chr3:93818800-93832000	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr3:93818800-93839800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr3:93819400-93844800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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