Variant report

Variant	rs73037444
Chromosome Location	chr1:169548449-169548450
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:51)

rs_ID	r²[population]
rs1557573	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16862358	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16862404	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2157583	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3917832	1.00[EUR][1000 genomes]
rs3917835	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3917844	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3917855	1.00[EUR][1000 genomes]
rs57207056	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57637273	0.85[AMR][1000 genomes]
rs58131257	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60345655	1.00[EUR][1000 genomes]
rs60781559	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60864119	1.00[EUR][1000 genomes]
rs724510	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73035543	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73035547	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73035573	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73037438	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74124515	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74124518	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9287094	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332478	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332479	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332480	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332482	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332483	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332485	1.00[EUR][1000 genomes]
rs9332486	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332488	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332489	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332490	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332491	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332492	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332493	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332494	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332496	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332498	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332499	1.00[EUR][1000 genomes]
rs9332501	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332506	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332508	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332515	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332518	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332524	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332527	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332530	1.00[EUR][1000 genomes]
rs9332532	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332539	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332565	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9332569	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv10418	chr1:169059628-169621268	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv548187	chr1:169530837-169559035	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv872534	chr1:169533266-169561274	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169533200-169551600	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr1:169541600-169550400	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr1:169542000-169550400	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr1:169542200-169554800	Weak transcription	Placenta	Placenta
5	chr1:169543800-169554200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr1:169545400-169549800	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr1:169546600-169548600	Weak transcription	Right Ventricle	heart
8	chr1:169547200-169549200	Enhancers	HepG2	liver
9	chr1:169548000-169550200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr1:169548400-169550200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr1:169548400-169550800	Genic enhancers	Liver	Liver

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