Variant report

Variant	rs1443262
Chromosome Location	chr17:66847193-66847194
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1373066	0.92[CEU][hapmap];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1443259	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1443261	0.92[CEU][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1470292	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1470293	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1470294	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1481	0.96[CEU][hapmap];0.97[EUR][1000 genomes]
rs1550646	0.83[EUR][1000 genomes]
rs1808919	0.92[AMR][1000 genomes]
rs1838100	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1838101	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1867235	0.94[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1978962	0.85[EUR][1000 genomes]
rs2083790	0.92[CEU][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2218350	0.92[CEU][hapmap];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2363753	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4246431	0.91[CEU][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4968826	0.92[CEU][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4968962	0.94[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4968967	0.92[CEU][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6501766	0.94[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6501767	0.94[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6501768	0.94[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6501799	0.81[AMR][1000 genomes]
rs6501813	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6501814	0.81[EUR][1000 genomes]
rs6501835	0.92[CEU][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6501839	0.92[CEU][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7209220	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7210022	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7211979	0.91[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7216817	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8068204	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8074944	0.91[CEU][hapmap];0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8078168	0.85[EUR][1000 genomes]
rs8080098	0.92[CEU][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8082619	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs894593	0.94[AMR][1000 genomes]
rs894594	0.92[CEU][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs980423	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9895868	0.94[AMR][1000 genomes];0.80[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	nsv1067334	chr17:66695039-67221585	Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv543411	chr17:66695039-67221585	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv908694	chr17:66802992-66913936	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:66845600-66850600	Enhancers	Fetal Muscle Leg	muscle
2	chr17:66845800-66847200	Enhancers	Adipose Nuclei	Adipose
3	chr17:66846000-66848000	Enhancers	Fetal Lung	lung
4	chr17:66846200-66847200	Enhancers	Fetal Stomach	stomach
5	chr17:66846200-66851200	Weak transcription	Fetal Muscle Trunk	muscle
6	chr17:66846400-66849400	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr17:66846800-66847200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr17:66846800-66847200	Enhancers	Rectal Smooth Muscle	rectum
9	chr17:66846800-66847400	Enhancers	Colon Smooth Muscle	Colon
10	chr17:66846800-66849000	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr17:66847000-66847400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr17:66847000-66847400	Weak transcription	Ovary	ovary
13	chr17:66847000-66849000	Weak transcription	NHDF-Ad	bronchial
14	chr17:66847000-66849200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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