Variant report

Variant	rs73062132
Chromosome Location	chr1:185878234-185878235
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:185872368..185875154-chr1:185878139..185880167,2	K562	blood:

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs10465478	1.00[EUR][1000 genomes]
rs10465499	1.00[EUR][1000 genomes]
rs12239587	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12239922	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12239929	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1322354	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1322355	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1322356	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13375391	1.00[EUR][1000 genomes]
rs16824645	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16824657	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16824658	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16824663	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16824665	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16824668	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16824669	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16824673	1.00[EUR][1000 genomes]
rs16824678	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16824688	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16824692	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16824719	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16824725	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16824726	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16824728	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16824729	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16824732	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16824736	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16824741	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16824744	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1951512	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1951513	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1951515	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1951516	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41533044	1.00[EUR][1000 genomes]
rs55678382	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55943726	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55975103	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56182901	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57103984	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs57289095	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs57454743	1.00[EUR][1000 genomes]
rs58063730	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58437418	1.00[EUR][1000 genomes]
rs59787112	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs59818099	0.93[AMR][1000 genomes]
rs61261990	1.00[EUR][1000 genomes]
rs6425008	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6664313	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6664384	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6666206	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6666950	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6667046	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6679622	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6679893	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6689494	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6689783	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6690968	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6701167	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6703739	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73054454	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73054465	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73056300	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73058203	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73058206	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73058209	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73058214	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73058224	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73058243	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73058250	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73062122	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73062125	0.90[AFR][1000 genomes]
rs73062134	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73062135	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73062140	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73062143	1.00[AMR][1000 genomes]
rs73062161	1.00[EUR][1000 genomes]
rs73062166	1.00[EUR][1000 genomes]
rs74134212	1.00[EUR][1000 genomes]
rs744737	1.00[EUR][1000 genomes]
rs7518783	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7544887	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9628634	1.00[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	nsv548398	chr1:185136458-186003094	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
2	esv3424090	chr1:185679718-186270877	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:185868000-185878400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:185872800-185878400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr1:185873000-185878400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr1:185873200-185880800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr1:185873400-185881200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr1:185875600-185895800	Weak transcription	NHDF-Ad	bronchial
7	chr1:185876800-185878400	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr1:185877000-185881000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:185877000-185894200	Weak transcription	Fetal Lung	lung
10	chr1:185877200-185881000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr1:185877800-185904400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr1:185878200-185878600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr1:185878200-185878600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr1:185878200-185878800	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr1:185878200-185878800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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