Variant report

Variant	rs72886577
Chromosome Location	chr2:183819091-183819092
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:183812719..183815141-chr2:183816615..183820380,4	K562	blood:
2	chr2:183804799..183806405-chr2:183817815..183819444,2	K562	blood:
3	chr2:183811184..183814871-chr2:183818695..183820986,3	K562	blood:
4	chr2:183816933..183819427-chr2:183831655..183834604,2	K562	blood:

Variant related genes	Relation type
ENSG00000061676	Chromatin interaction

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs1473614	0.86[EUR][1000 genomes]
rs1473615	0.86[EUR][1000 genomes]
rs1473616	0.86[EUR][1000 genomes]
rs2675054	0.86[EUR][1000 genomes]
rs2705715	0.86[EUR][1000 genomes]
rs2705718	0.86[EUR][1000 genomes]
rs2705719	0.86[EUR][1000 genomes]
rs2705720	0.86[EUR][1000 genomes]
rs2705721	0.86[EUR][1000 genomes]
rs35142583	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36077496	1.00[AMR][1000 genomes]
rs55657876	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs55696219	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs55707150	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs55764044	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs55957340	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56152140	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56182353	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6707761	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6712479	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6743323	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6750392	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72886518	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72886527	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72886538	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72886541	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72886545	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72886547	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72886553	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72886557	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72886568	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72886596	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72886597	0.89[AFR][1000 genomes]
rs72886600	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72888431	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72888449	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72888452	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72888461	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72888464	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72888472	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72888474	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72888478	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72888481	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72888488	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72888489	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72890307	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72890345	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72890349	0.87[AMR][1000 genomes]
rs72890352	1.00[AMR][1000 genomes]
rs72890353	1.00[AMR][1000 genomes]
rs72890370	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72890384	1.00[AMR][1000 genomes]
rs72890392	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72890398	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72892604	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72892631	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72892638	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72892656	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72892689	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72892694	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72892702	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72894503	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72894513	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72894523	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72894527	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72894533	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72894535	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72894537	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72894539	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72894544	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72894546	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72894570	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72894585	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72894593	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72894596	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72896508	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72896517	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72896518	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72896520	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72896524	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72896528	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72896534	0.86[EUR][1000 genomes]
rs72900766	1.00[AMR][1000 genomes]
rs72900772	1.00[AMR][1000 genomes]
rs72900775	1.00[AMR][1000 genomes]
rs72900780	1.00[AMR][1000 genomes]
rs7562034	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7565260	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7566497	1.00[AMR][1000 genomes]
rs7567370	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7577407	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7597417	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 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	esv2757842	chr2:183437700-183835084	Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv2759104	chr2:183437700-183835084	Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv818096	chr2:183701588-183827018	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	esv3693446	chr2:183785598-183833514	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
6	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

No data

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183773400-183866000	Weak transcription	Colonic Mucosa	Colon
2	chr2:183773400-183877800	Weak transcription	Stomach Mucosa	stomach
3	chr2:183775600-183833000	Weak transcription	Pancreas	Pancrea
4	chr2:183780400-183874800	Weak transcription	Esophagus	oesophagus
5	chr2:183785800-183824200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:183786600-183826600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr2:183787000-183824000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
8	chr2:183788000-183830000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:183788200-183845600	Weak transcription	Lung	lung
10	chr2:183789200-183836400	Weak transcription	Brain Cingulate Gyrus	brain
11	chr2:183790800-183824200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr2:183793400-183840800	Weak transcription	Fetal Brain Male	brain
13	chr2:183793600-183823800	Strong transcription	HUES48 Cell Line	embryonic stem cell
14	chr2:183793600-183826600	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr2:183795200-183824200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
16	chr2:183795400-183857600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr2:183798600-183847000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr2:183803800-183826600	Weak transcription	Brain Germinal Matrix	brain
19	chr2:183803800-183826600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr2:183804800-183859600	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr2:183805600-183874400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr2:183807400-183824200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr2:183812000-183819600	Weak transcription	Brain Substantia Nigra	brain
24	chr2:183812000-183821200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr2:183812000-183839000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:183812000-183857800	Weak transcription	Rectal Smooth Muscle	rectum
27	chr2:183812200-183819600	Weak transcription	Right Atrium	heart
28	chr2:183812200-183820400	Weak transcription	Stomach Smooth Muscle	stomach
29	chr2:183812200-183826200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr2:183812200-183826200	Weak transcription	Left Ventricle	heart
31	chr2:183812200-183826600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr2:183812200-183832800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr2:183812200-183833000	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr2:183812200-183838200	Weak transcription	Small Intestine	intestine
35	chr2:183812200-183842000	Weak transcription	Right Ventricle	heart
36	chr2:183812200-183874800	Weak transcription	Gastric	stomach
37	chr2:183812400-183831200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr2:183812400-183856800	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr2:183813200-183819600	Strong transcription	HepG2	liver
40	chr2:183813400-183823200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr2:183813600-183823800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr2:183814400-183823600	Strong transcription	Adipose Nuclei	Adipose
43	chr2:183814600-183819200	Weak transcription	Brain Angular Gyrus	brain
44	chr2:183814600-183874800	Weak transcription	Aorta	Aorta
45	chr2:183814600-183893600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr2:183814800-183819600	Weak transcription	Brain Hippocampus Middle	brain
47	chr2:183814800-183821200	Weak transcription	Hela-S3	cervix
48	chr2:183814800-183824000	Strong transcription	HUES6 Cell Line	embryonic stem cell
49	chr2:183814800-183845600	Weak transcription	Ovary	ovary
50	chr2:183815000-183819600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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