Variant report

Variant	rs1202828
Chromosome Location	chr1:58352716-58352717
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1022636	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1202794	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1202797	0.91[ASN][1000 genomes]
rs1202798	0.85[CEU][hapmap];0.88[CHB][hapmap]
rs1202799	0.85[CEU][hapmap];0.88[CHB][hapmap]
rs1202800	0.91[ASN][1000 genomes]
rs1202801	0.84[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs1202804	0.84[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs1202808	0.91[ASN][1000 genomes]
rs1202809	0.91[ASN][1000 genomes]
rs1202811	0.84[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs1202829	1.00[CEU][hapmap];0.88[CHB][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1202830	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1202833	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1202834	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1202835	1.00[CEU][hapmap];0.88[CHB][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1202836	0.80[EUR][1000 genomes]
rs1202837	1.00[CEU][hapmap];0.88[CHB][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1202839	1.00[CEU][hapmap];0.85[CHB][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1202840	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1202841	1.00[CEU][hapmap];0.88[CHB][hapmap];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1202842	0.94[CEU][hapmap];1.00[CHB][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1202845	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1202846	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1202847	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2057225	1.00[JPT][hapmap]
rs2749274	1.00[CEU][hapmap];0.86[CHB][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2749275	0.95[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2749276	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][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	nsv1015057	chr1:57976993-58793962	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv530017	chr1:58002290-58669736	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv431379	chr1:58224212-58802608	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv829937	chr1:58258288-58406506	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1008205	chr1:58349005-58375261	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:58347800-58359600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:58348200-58353400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr1:58349400-58355600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:58349600-58355400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr1:58350000-58353400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:58350600-58373800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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