Variant report

Variant	rs10911878
Chromosome Location	chr1:186506889-186506890
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:186501486..186504451-chr1:186506329..186509291,2	K562	blood:
2	chr1:186344658..186346802-chr1:186505094..186507834,3	K562	blood:
3	chr1:186344658..186346288-chr1:186505094..186507834,2	K562	blood:

Variant related genes	Relation type
ENSG00000157181	Chromatin interaction
ENSG00000047410	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10798041	0.93[CEU][hapmap]
rs10798048	0.93[CEU][hapmap];0.84[YRI][hapmap]
rs10798051	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10911861	0.86[CEU][hapmap]
rs10911863	0.84[CEU][hapmap]
rs10911866	0.93[CEU][hapmap]
rs10911876	1.00[CEU][hapmap]
rs10911877	0.87[CEU][hapmap];0.88[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10911886	0.93[CEU][hapmap];0.81[YRI][hapmap]
rs10911888	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10911890	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10911892	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10911895	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10911904	0.86[CEU][hapmap]
rs10911905	0.85[CEU][hapmap]
rs1108635	0.81[ASN][1000 genomes]
rs1119231	0.87[CEU][hapmap]
rs11580808	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11582183	0.82[CEU][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11583191	0.86[CEU][hapmap]
rs11805124	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11808643	0.81[ASN][1000 genomes]
rs12057695	0.93[CEU][hapmap]
rs12081510	1.00[CEU][hapmap]
rs12087470	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12093901	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12402521	0.83[CEU][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12404145	1.00[CEU][hapmap]
rs12407957	0.93[CEU][hapmap]
rs12728706	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12731288	0.81[ASN][1000 genomes]
rs12750371	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1799957	0.83[CEU][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1882926	0.86[CEU][hapmap]
rs1929092	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2024761	0.83[CEU][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs20417	0.87[CEU][hapmap]
rs2066826	0.93[CEU][hapmap]
rs2143416	0.86[CEU][hapmap]
rs2143417	0.86[CEU][hapmap]
rs2179555	0.86[CEU][hapmap]
rs2180167	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2207727	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2383508	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2891247	0.93[CEU][hapmap]
rs34396375	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35066734	0.86[CEU][hapmap]
rs35206897	0.82[ASN][1000 genomes]
rs35643079	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs36105782	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3844242	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3901950	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4140433	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4567244	0.80[CEU][hapmap];0.84[YRI][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4648276	0.93[CEU][hapmap]
rs59547074	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6425035	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6659683	0.83[CEU][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6666413	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6666813	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6672638	0.86[CEU][hapmap]
rs6672836	0.82[CEU][hapmap];0.84[YRI][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6675505	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6677346	0.83[CEU][hapmap];0.84[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6680252	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6689065	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6689727	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6694957	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7512750	0.93[CEU][hapmap];0.81[YRI][hapmap]
rs7518525	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7536199	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7556360	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004481	chr1:186095854-186750968	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv535223	chr1:186095854-186750968	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	nsv1012164	chr1:186323867-186565995	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	esv2762201	chr1:186323879-186566007	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv832059	chr1:186464932-186639125	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:186503600-186507600	Enhancers	NHDF-Ad	bronchial
2	chr1:186503800-186508000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:186504000-186507200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr1:186504000-186507400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr1:186504600-186507400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr1:186504800-186510200	Weak transcription	Right Atrium	heart
7	chr1:186506000-186507000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr1:186506000-186507600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr1:186506400-186509600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:186506400-186512200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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