Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11100236	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11100243	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11732099	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12645160	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12646752	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12648292	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1393576	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17239575	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28453123	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs55650126	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55993310	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs56032650	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs56234927	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs60517538	0.92[EUR][1000 genomes]
rs62339597	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6826002	0.87[EUR][1000 genomes]
rs6853778	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7654634	0.87[EUR][1000 genomes]
rs7692467	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7693162	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs961786	0.89[AMR][1000 genomes];0.94[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	nsv1015469	chr4:160389277-160841619	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv537316	chr4:160389277-160841619	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv881205	chr4:160516090-160628006	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160508600-160526800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:160516200-160526800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr4:160516800-160530000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:160519600-160527600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr4:160519600-160528200	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr4:160520000-160525800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:160520000-160527000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr4:160520400-160526800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:160521200-160524200	Weak transcription	Fetal Intestine Large	intestine
10	chr4:160521400-160525800	Weak transcription	Fetal Kidney	kidney
11	chr4:160524000-160524600	Enhancers	Fetal Intestine Small	intestine

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