Variant report

Variant	rs4558042
Chromosome Location	chr1:170280091-170280092
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1034185	1.00[ASN][1000 genomes]
rs10494487	1.00[ASN][1000 genomes]
rs10919349	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10919378	1.00[ASN][1000 genomes]
rs10919379	1.00[ASN][1000 genomes]
rs10919382	1.00[ASN][1000 genomes]
rs1113231	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.82[MEX][hapmap];0.81[TSI][hapmap]
rs11586686	1.00[ASN][1000 genomes]
rs12116910	1.00[CHB][hapmap]
rs12121358	1.00[ASN][1000 genomes]
rs12126109	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12127149	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12128082	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12129359	1.00[ASN][1000 genomes]
rs12130105	1.00[ASN][1000 genomes]
rs12132288	1.00[ASN][1000 genomes]
rs12132402	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12135696	1.00[ASN][1000 genomes]
rs12137241	1.00[ASN][1000 genomes]
rs12138644	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12139302	1.00[ASN][1000 genomes]
rs12141935	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12143611	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12407889	1.00[ASN][1000 genomes]
rs12408130	1.00[ASN][1000 genomes]
rs12732119	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12734846	1.00[ASN][1000 genomes]
rs12748912	1.00[ASN][1000 genomes]
rs12753359	1.00[ASN][1000 genomes]
rs1332963	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1332964	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1333142	1.00[CHB][hapmap]
rs1537390	1.00[CHB][hapmap]
rs17346122	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17346171	1.00[ASN][1000 genomes]
rs17350179	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17350305	0.91[ASN][1000 genomes]
rs1999523	1.00[CHB][hapmap]
rs2095135	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28436845	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34161857	1.00[ASN][1000 genomes]
rs34860969	1.00[ASN][1000 genomes]
rs35084451	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35833908	1.00[ASN][1000 genomes]
rs4256872	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4300285	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4489621	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4575137	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4578264	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6657395	1.00[ASN][1000 genomes]
rs6667077	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6667462	0.90[ASN][1000 genomes]
rs6684260	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6698352	1.00[CHB][hapmap];0.89[GIH][hapmap];0.82[MEX][hapmap]
rs7516510	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7534693	1.00[ASN][1000 genomes]
rs7537355	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014033	chr1:169968488-170453021	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
2	nsv535200	chr1:169968488-170453021	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
3	nsv872543	chr1:170171083-170674903	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv533915	chr1:170258766-170725296	Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:170276200-170280400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr1:170278200-170280400	Enhancers	Osteobl	bone
3	chr1:170278200-170280600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:170278400-170280200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr1:170278400-170280400	Enhancers	Fetal Muscle Leg	muscle
6	chr1:170279000-170280200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr1:170279000-170280600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:170279000-170280600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr1:170279200-170284000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:170279400-170280200	Enhancers	NHLF	lung
11	chr1:170279400-170284000	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr1:170279600-170281000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:170279800-170280200	Enhancers	NH-A	brain
14	chr1:170279800-170282600	Weak transcription	Adipose Nuclei	Adipose
15	chr1:170279800-170284000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:170280000-170282400	Enhancers	NHDF-Ad	bronchial
17	chr1:170280000-170285200	Weak transcription	Placenta Amnion	Placenta Amnion

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