Variant report

Variant	rs73579483
Chromosome Location	chr6:146012113-146012114
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 121 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:120)

rs_ID	r²[population]
rs12111090	0.96[AFR][1000 genomes]
rs12111476	0.96[AFR][1000 genomes]
rs1591698	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs28479261	0.93[AFR][1000 genomes]
rs28587324	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs28829296	0.94[AFR][1000 genomes]
rs4896845	0.84[AFR][1000 genomes]
rs4896847	0.84[AFR][1000 genomes]
rs55658016	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs55746945	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs55813779	0.95[AFR][1000 genomes]
rs55814547	0.95[AFR][1000 genomes]
rs55820518	0.90[AFR][1000 genomes]
rs56116838	0.96[AFR][1000 genomes]
rs56198487	0.89[AFR][1000 genomes]
rs56282473	0.95[AFR][1000 genomes]
rs56864636	0.90[AFR][1000 genomes]
rs56950953	0.95[AFR][1000 genomes]
rs57105639	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs57646957	0.93[AFR][1000 genomes]
rs58588227	0.89[AFR][1000 genomes]
rs59135568	0.96[AFR][1000 genomes]
rs59557516	0.93[AFR][1000 genomes]
rs60162832	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs60609437	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs61014905	0.93[AFR][1000 genomes]
rs61041405	0.92[AFR][1000 genomes]
rs61121433	0.96[AFR][1000 genomes]
rs6570702	0.96[AFR][1000 genomes]
rs6570707	0.96[AFR][1000 genomes]
rs6570709	0.96[AFR][1000 genomes]
rs6570710	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6570714	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6570720	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6900158	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6901219	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6901587	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6902273	0.96[AFR][1000 genomes]
rs6902358	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6902952	0.99[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6908707	0.95[AFR][1000 genomes]
rs6913497	0.99[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6914491	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6918350	0.96[AFR][1000 genomes]
rs6918739	0.93[AFR][1000 genomes]
rs6919173	0.96[AFR][1000 genomes]
rs6920248	0.90[AFR][1000 genomes]
rs6921110	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6927960	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6928780	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6930335	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6931280	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6940415	0.99[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73564486	0.93[AFR][1000 genomes]
rs73566113	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73566115	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73566121	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73566126	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73566139	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73566140	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73566157	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73566168	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73566721	0.91[AFR][1000 genomes]
rs73566724	0.93[AFR][1000 genomes]
rs73566728	0.93[AFR][1000 genomes]
rs73566742	0.93[AFR][1000 genomes]
rs73566747	0.93[AFR][1000 genomes]
rs73566751	0.93[AFR][1000 genomes]
rs73566754	0.93[AFR][1000 genomes]
rs73566757	0.92[AFR][1000 genomes]
rs73568127	0.89[AFR][1000 genomes]
rs73568130	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73568133	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73568134	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73568138	0.89[AFR][1000 genomes]
rs73568145	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73568148	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73568151	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73568185	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73568188	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73568362	0.95[AFR][1000 genomes]
rs73568366	0.95[AFR][1000 genomes]
rs73568375	0.95[AFR][1000 genomes]
rs73568389	0.88[AFR][1000 genomes]
rs73577358	0.96[AFR][1000 genomes]
rs73577363	0.96[AFR][1000 genomes]
rs73577384	0.96[AFR][1000 genomes]
rs73579478	0.95[AFR][1000 genomes]
rs73579498	0.99[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73782053	0.99[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73782068	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73784038	0.93[AFR][1000 genomes]
rs73784067	0.95[AFR][1000 genomes]
rs7738406	0.95[AFR][1000 genomes]
rs7738822	0.95[AFR][1000 genomes]
rs7738906	0.95[AFR][1000 genomes]
rs7741139	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7744082	0.99[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7745379	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7745722	0.98[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7749377	0.84[AFR][1000 genomes]
rs7750382	0.93[AFR][1000 genomes]
rs7753694	0.96[AFR][1000 genomes]
rs7753832	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7754367	0.90[AFR][1000 genomes]
rs7757137	0.89[AFR][1000 genomes]
rs7758839	0.99[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7759254	0.92[AFR][1000 genomes]
rs7761251	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7761577	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7763273	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7768195	0.95[AFR][1000 genomes]
rs7771112	0.82[AFR][1000 genomes]
rs7771653	0.93[AFR][1000 genomes]
rs7772012	0.96[AFR][1000 genomes]
rs7772550	0.95[AFR][1000 genomes]
rs7773780	0.94[AFR][1000 genomes]
rs9718033	0.85[AFR][1000 genomes]
rs9766595	0.94[AFR][1000 genomes]
rs9766596	0.95[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934064	chr6:146007547-146044233	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145995200-146013200	Weak transcription	Pancreas	Pancrea
2	chr6:146001800-146012200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr6:146003400-146033600	Weak transcription	Brain Hippocampus Middle	brain
4	chr6:146003600-146020600	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr6:146003600-146029400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:146003800-146012200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr6:146003800-146012400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr6:146003800-146026600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr6:146003800-146029600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr6:146003800-146029600	Weak transcription	Ovary	ovary
11	chr6:146006800-146014800	Weak transcription	Adipose Nuclei	Adipose
12	chr6:146006800-146050000	Weak transcription	Brain Cingulate Gyrus	brain
13	chr6:146007000-146022400	Weak transcription	Primary B cells from cord blood	blood
14	chr6:146007400-146043800	Weak transcription	Liver	Liver
15	chr6:146007800-146013600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:146008600-146015600	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr6:146009600-146022400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:146010000-146012200	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr6:146011200-146020000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:146011200-146029600	Weak transcription	Aorta	Aorta
21	chr6:146012000-146012600	Enhancers	HepG2	liver

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