Variant report

Variant	rs6658592
Chromosome Location	chr1:185979191-185979192
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:185976975..185979218-chr1:185981413..185983936,2	MCF-7	breast:
2	chr1:185974978..185977971-chr1:185978048..185981711,3	K562	blood:

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10158272	0.80[AFR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10737266	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10752958	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10752959	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10798028	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10798030	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10798031	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10798032	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10798033	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10798034	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10911799	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10911805	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10911806	0.83[AFR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10911807	0.87[AFR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10911808	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12091407	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12129650	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12144523	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12566113	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1540925	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1569989	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2024901	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2070282	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2208084	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2208085	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2224276	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2224277	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3795406	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4141459	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4626827	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4650689	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4650690	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4650691	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4650692	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4650693	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4651290	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4651291	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4651292	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4651293	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6425012	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6425013	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6425014	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6658929	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6659819	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6665753	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6679262	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6684429	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6698240	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs743136	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs743137	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs743138	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7512909	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7520459	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7522627	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7535056	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7541013	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7544709	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs980947	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][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:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:185936600-185999000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:185938800-185990200	Weak transcription	Liver	Liver
3	chr1:185938800-185994600	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr1:185939000-185986000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr1:185939200-186023000	Weak transcription	Adipose Nuclei	Adipose
6	chr1:185959000-185979200	Weak transcription	Esophagus	oesophagus
7	chr1:185960200-185999000	Weak transcription	Fetal Lung	lung
8	chr1:185964200-186014800	Weak transcription	Lung	lung
9	chr1:185965800-185983200	Weak transcription	NHDF-Ad	bronchial
10	chr1:185972200-185983600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:185977600-185979200	Enhancers	Osteobl	bone
12	chr1:185978200-185979400	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr1:185978400-185979400	Enhancers	Primary hematopoietic stem cells	blood
14	chr1:185978400-185980600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:185978600-185979200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr1:185978600-185979200	Enhancers	HUVEC	blood vessel
17	chr1:185978600-185983600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr1:185978800-185981800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr1:185978800-185982800	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr1:185978800-185983000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:185978800-185983200	Weak transcription	NH-A	brain
22	chr1:185979000-185979200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr1:185979000-185979200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr1:185979000-185979200	Enhancers	Aorta	Aorta
25	chr1:185979000-185979400	Enhancers	Left Ventricle	heart

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