Variant report

Variant	rs72968432
Chromosome Location	chr4:107083497-107083498
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 107 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs11933976	1.00[AMR][1000 genomes]
rs11936261	1.00[AMR][1000 genomes]
rs11936375	1.00[AMR][1000 genomes]
rs17036551	1.00[AMR][1000 genomes]
rs17036571	1.00[AMR][1000 genomes]
rs1988966	0.84[AFR][1000 genomes]
rs2230255	0.82[AFR][1000 genomes]
rs56100035	1.00[AMR][1000 genomes]
rs56208962	1.00[AMR][1000 genomes]
rs56727772	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56761478	1.00[AMR][1000 genomes]
rs57139070	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58874453	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59703105	1.00[AMR][1000 genomes]
rs60169642	1.00[AMR][1000 genomes]
rs60697569	1.00[AMR][1000 genomes]
rs60782919	1.00[AMR][1000 genomes]
rs61008564	1.00[AMR][1000 genomes]
rs6818599	1.00[AMR][1000 genomes]
rs72876572	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72876587	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72876596	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72878503	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72878506	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72878508	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72878520	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72878531	0.84[AFR][1000 genomes]
rs72878534	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72878535	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72878538	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72878541	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72878545	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72878548	0.89[AFR][1000 genomes]
rs72878554	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72878555	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72878559	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72878578	0.82[AFR][1000 genomes]
rs72878581	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72878592	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72878594	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72880210	1.00[AMR][1000 genomes]
rs72891619	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891621	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891622	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891625	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891627	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891632	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891640	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891645	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891650	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891660	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891662	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891664	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891668	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891675	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891682	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891685	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72891700	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72893604	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72893607	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72893622	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72893630	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72958897	0.85[AFR][1000 genomes]
rs72960676	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72960686	1.00[AMR][1000 genomes]
rs72962513	1.00[AMR][1000 genomes]
rs72962516	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72962593	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72962597	0.98[AFR][1000 genomes]
rs72962598	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72962600	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72962601	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72964404	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72964407	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72964409	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72964415	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72964420	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72964437	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72964439	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72964441	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72964454	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72964460	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72964465	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72964475	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72964479	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72964485	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72964491	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72968407	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72968409	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72968436	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72968440	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72968441	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72968449	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73836955	1.00[AMR][1000 genomes]
rs7661620	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879701	chr4:107024776-107163128	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv508301	chr4:107049086-107092730	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	esv1799357	chr4:107058025-107099737	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv1801434	chr4:107058025-107099737	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv1800933	chr4:107058025-107118662	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv1802243	chr4:107058025-107118662	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv1802962	chr4:107058025-107118662	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv1803376	chr4:107058025-107118662	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	esv1848076	chr4:107058334-107118662	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	esv1851828	chr4:107059549-107118662	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv879702	chr4:107065718-107175191	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv879703	chr4:107082926-107163128	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:107038000-107112000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr4:107053800-107083800	Weak transcription	Left Ventricle	heart
3	chr4:107053800-107101600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr4:107054000-107091000	Weak transcription	Stomach Smooth Muscle	stomach
5	chr4:107054000-107113600	Weak transcription	Brain Anterior Caudate	brain
6	chr4:107066400-107151200	Weak transcription	Colon Smooth Muscle	Colon
7	chr4:107067400-107083600	Weak transcription	Fetal Kidney	kidney
8	chr4:107068600-107083600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:107070600-107084200	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr4:107071800-107176400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr4:107073000-107086800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr4:107074200-107114400	Weak transcription	NHDF-Ad	bronchial
13	chr4:107074600-107111800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr4:107075200-107091000	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr4:107075800-107114000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr4:107075800-107118200	Weak transcription	Brain Substantia Nigra	brain
17	chr4:107075800-107129600	Weak transcription	Spleen	Spleen
18	chr4:107076000-107083800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr4:107076400-107083600	Weak transcription	Primary B cells from peripheral blood	blood
20	chr4:107076400-107114200	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr4:107076800-107083600	Weak transcription	Thymus	Thymus
22	chr4:107077000-107089600	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr4:107078000-107083600	Weak transcription	Dnd41	blood
24	chr4:107078000-107083800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr4:107078000-107107800	Weak transcription	HSMMtube	muscle
26	chr4:107078200-107116000	Weak transcription	Colonic Mucosa	Colon
27	chr4:107078600-107084200	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr4:107078800-107112200	Weak transcription	Osteobl	bone
29	chr4:107078800-107114200	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr4:107081800-107083600	Strong transcription	HepG2	liver
31	chr4:107082400-107085000	Strong transcription	Fetal Thymus	thymus
32	chr4:107082600-107083600	ZNF genes & repeats	Fetal Intestine Large	intestine
33	chr4:107082600-107084000	ZNF genes & repeats	Fetal Brain Female	brain
34	chr4:107082600-107084800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr4:107082600-107085600	Strong transcription	Primary B cells from cord blood	blood
36	chr4:107082800-107084000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr4:107082800-107084200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
38	chr4:107082800-107084200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
39	chr4:107082800-107085400	Strong transcription	Primary T cells from cord blood	blood
40	chr4:107082800-107086800	Weak transcription	Fetal Heart	heart
41	chr4:107083000-107083600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
42	chr4:107083000-107084000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:107083000-107084000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr4:107083000-107084600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr4:107083000-107084800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr4:107083000-107085000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr4:107083200-107083600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr4:107083200-107083600	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
49	chr4:107083200-107083600	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
50	chr4:107083200-107083800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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