Variant report

Variant	rs73118201
Chromosome Location	chr1:223355072-223355073
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs11485988	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11488551	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1640803	0.87[EUR][1000 genomes]
rs1773753	1.00[EUR][1000 genomes]
rs2160152	0.87[EUR][1000 genomes]
rs34071437	1.00[AMR][1000 genomes]
rs35169648	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35227692	1.00[AMR][1000 genomes]
rs35412940	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35551279	1.00[AMR][1000 genomes]
rs35644560	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35778136	1.00[AMR][1000 genomes]
rs5744122	1.00[AMR][1000 genomes]
rs712862	0.87[EUR][1000 genomes]
rs73118152	1.00[AMR][1000 genomes]
rs73118166	0.87[EUR][1000 genomes]
rs73118168	0.87[EUR][1000 genomes]
rs73118170	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73118175	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73118176	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73118177	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73118181	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73118186	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73118187	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73118190	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73118193	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73118194	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73118198	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73118202	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73120203	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73120204	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73120206	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73120207	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73120214	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73120219	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73120222	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73120224	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73120229	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73120232	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73120234	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73120236	1.00[AMR][1000 genomes]
rs73120250	1.00[AMR][1000 genomes]
rs73120257	1.00[AMR][1000 genomes]
rs73120261	1.00[AMR][1000 genomes]
rs73120265	1.00[AMR][1000 genomes]
rs73120297	1.00[AMR][1000 genomes]
rs851140	0.87[EUR][1000 genomes]
rs851144	0.87[EUR][1000 genomes]
rs851146	0.87[EUR][1000 genomes]
rs851147	0.87[EUR][1000 genomes]
rs851151	0.87[EUR][1000 genomes]
rs851156	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012537	chr1:222755091-223512243	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv832659	chr1:223294767-223438487	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223347800-223357600	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr1:223348800-223355400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
3	chr1:223349800-223375400	Weak transcription	Right Atrium	heart
4	chr1:223350000-223355800	Enhancers	Fetal Thymus	thymus
5	chr1:223350200-223355400	Enhancers	Liver	Liver
6	chr1:223352800-223358600	Enhancers	Primary T cells from cord blood	blood
7	chr1:223353000-223362000	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr1:223353200-223356200	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr1:223353400-223355200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:223353400-223355400	Weak transcription	Esophagus	oesophagus
11	chr1:223353400-223355600	Enhancers	Stomach Mucosa	stomach
12	chr1:223353600-223355200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr1:223353800-223355200	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr1:223353800-223357200	Enhancers	HMEC	breast
15	chr1:223354000-223355400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr1:223354400-223355400	Enhancers	Pancreas	Pancrea
17	chr1:223354400-223355600	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr1:223354400-223357200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr1:223354400-223357600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr1:223355000-223356400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr1:223355000-223356400	Weak transcription	NHDF-Ad	bronchial
22	chr1:223355000-223356600	Weak transcription	NHEK	skin

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