Variant report

Variant	rs72896528
Chromosome Location	chr2:184028964-184028965
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:183998810..184000982-chr2:184027517..184029612,2	K562	blood:
2	chr2:183988386..183991369-chr2:184028228..184030386,3	K562	blood:
3	chr2:183988386..183990737-chr2:184027696..184029728,3	K562	blood:

Variant related genes	Relation type
ENSG00000163002	Chromatin interaction

Extended variants
information (count: 126 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:119)

rs_ID	r²[population]
rs1473614	1.00[EUR][1000 genomes]
rs1473615	1.00[EUR][1000 genomes]
rs1473616	1.00[EUR][1000 genomes]
rs2675053	0.92[EUR][1000 genomes]
rs2675054	1.00[EUR][1000 genomes]
rs2705715	1.00[EUR][1000 genomes]
rs2705718	1.00[EUR][1000 genomes]
rs2705719	1.00[EUR][1000 genomes]
rs2705720	1.00[EUR][1000 genomes]
rs2705721	1.00[EUR][1000 genomes]
rs35142583	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs55657876	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55678810	0.86[AMR][1000 genomes]
rs55696219	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55707150	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55764044	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55957340	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56152140	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56182353	0.88[EUR][1000 genomes]
rs6712479	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6722457	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6743323	0.88[EUR][1000 genomes]
rs6750392	0.88[EUR][1000 genomes]
rs72886547	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72886553	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72886557	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72886568	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72886577	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72886596	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72886600	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72888431	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72888449	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72888452	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72888461	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72888464	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72888472	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72888474	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72888478	0.86[EUR][1000 genomes]
rs72888481	0.86[EUR][1000 genomes]
rs72888488	0.86[EUR][1000 genomes]
rs72888489	0.86[EUR][1000 genomes]
rs72890307	0.88[EUR][1000 genomes]
rs72890345	0.97[EUR][1000 genomes]
rs72890349	0.90[EUR][1000 genomes]
rs72890352	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72890353	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72890370	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72890384	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs72890392	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72890398	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72892604	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72892631	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72892638	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72892656	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72892689	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72892694	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72892702	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72894503	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72894513	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72894523	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72894527	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72894533	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72894535	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72894537	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72894539	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72894544	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72894546	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72894570	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72894585	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72894593	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72894596	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72896508	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72896517	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72896518	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72896520	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72896524	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72896534	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72896555	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72896556	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72896558	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72896559	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72896560	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72896567	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72896581	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72896586	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72896598	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898507	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898512	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898513	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898514	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898516	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898517	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898522	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898525	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898529	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898532	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898535	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898538	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72898539	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898542	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898545	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72898548	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898555	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898558	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898562	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72898566	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898569	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898573	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898574	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898578	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72898581	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72898584	0.86[EUR][1000 genomes]
rs72898600	0.86[AMR][1000 genomes]
rs72900543	0.86[AMR][1000 genomes]
rs7562034	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7565260	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7567370	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7577407	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7597417	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009882	chr2:183213152-184171519	Weak transcription Strong transcription Flanking Active TSS 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 miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv1005281	chr2:183803173-184093877	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv875485	chr2:183827018-184195265	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv1010799	chr2:183855680-184244721	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv536072	chr2:183855680-184244721	Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	esv2763287	chr2:183939173-184037893	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv875486	chr2:184016627-184095979	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183990000-184050000	Weak transcription	Aorta	Aorta
2	chr2:183990200-184036400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:183990800-184031000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr2:183991000-184030400	Weak transcription	Brain Hippocampus Middle	brain
5	chr2:183991000-184048400	Weak transcription	Brain Angular Gyrus	brain
6	chr2:183991000-184053400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr2:183991000-184055400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr2:183991200-184035400	Weak transcription	Fetal Brain Male	brain
9	chr2:183991400-184034000	Weak transcription	NHLF	lung
10	chr2:183991400-184049600	Weak transcription	NHDF-Ad	bronchial
11	chr2:183991600-184029600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr2:183992400-184047600	Weak transcription	Hela-S3	cervix
13	chr2:184009000-184043800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:184009200-184034000	Weak transcription	Esophagus	oesophagus
15	chr2:184009200-184043600	Weak transcription	Psoas Muscle	Psoas
16	chr2:184009200-184048400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr2:184009400-184047200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr2:184014200-184031400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr2:184014600-184030800	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr2:184015000-184029000	Weak transcription	HSMMtube	muscle
21	chr2:184015000-184062000	Weak transcription	Small Intestine	intestine
22	chr2:184016000-184030400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr2:184016200-184030800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr2:184018400-184047400	Weak transcription	Pancreas	Pancrea
25	chr2:184019000-184031200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr2:184019000-184036600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr2:184019000-184043600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr2:184019000-184050000	Weak transcription	Gastric	stomach
29	chr2:184019000-184053400	Weak transcription	Placenta	Placenta
30	chr2:184019400-184030800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr2:184021000-184029200	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr2:184021200-184029000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr2:184021600-184029400	Strong transcription	K562	blood
34	chr2:184022000-184029000	Strong transcription	Primary T helper cells PMA-I stimulated	--
35	chr2:184022000-184029400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr2:184022000-184029400	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr2:184022000-184029600	Strong transcription	Primary B cells from cord blood	blood
38	chr2:184022000-184029600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr2:184022000-184029600	Strong transcription	Duodenum Mucosa	Duodenum
40	chr2:184022000-184030000	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr2:184022000-184031200	Strong transcription	Dnd41	blood
42	chr2:184022400-184030800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:184022600-184029200	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr2:184022600-184030400	Strong transcription	Liver	Liver
45	chr2:184022800-184029600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr2:184023000-184029200	Strong transcription	HepG2	liver
47	chr2:184023000-184029400	Strong transcription	Adipose Nuclei	Adipose
48	chr2:184023000-184029600	Strong transcription	Primary T cells fromperipheralblood	blood
49	chr2:184023000-184031400	Strong transcription	Fetal Thymus	thymus
50	chr2:184023000-184033000	Strong transcription	Primary T cells from cord blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links