Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10450962	0.80[EUR][1000 genomes]
rs10519023	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10851670	0.93[EUR][1000 genomes]
rs1108436	1.00[EUR][1000 genomes]
rs1559773	1.00[EUR][1000 genomes]
rs1648246	1.00[EUR][1000 genomes]
rs1680231	1.00[EUR][1000 genomes]
rs16942049	1.00[EUR][1000 genomes]
rs16942061	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16942101	0.80[EUR][1000 genomes]
rs2414658	0.93[EUR][1000 genomes]
rs2554006	1.00[EUR][1000 genomes]
rs2899653	1.00[EUR][1000 genomes]
rs2899654	1.00[EUR][1000 genomes]
rs335801	0.80[EUR][1000 genomes]
rs335810	0.80[EUR][1000 genomes]
rs57020611	1.00[EUR][1000 genomes]
rs59280158	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7171231	0.93[EUR][1000 genomes]
rs73427232	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8023442	1.00[EUR][1000 genomes]
rs986694	0.93[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	nsv904280	chr15:60042722-60524025	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv833028	chr15:60227565-60418112	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv569607	chr15:60303749-60347452	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1043235	chr15:60318001-60350625	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1044105	chr15:60318001-60354519	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr15:60316400-60318400	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr15:60316400-60319200	Enhancers	Ovary	ovary
3	chr15:60316600-60318600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr15:60316800-60318200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr15:60317200-60318200	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr15:60317200-60318400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr15:60317200-60318400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr15:60317200-60318400	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr15:60317200-60318600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr15:60317400-60318200	Enhancers	H1 Cell Line	embryonic stem cell
11	chr15:60317400-60318200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr15:60317600-60318400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr15:60317800-60324200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr15:60318000-60318200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr15:60318000-60318200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr15:60318000-60318200	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr15:60318000-60319200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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