Variant report

Variant	rs914656
Chromosome Location	chr9:16321008-16321009
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10217707	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10962376	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10962378	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12351741	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12351743	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12683271	0.84[EUR][1000 genomes]
rs12686344	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72714923	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949463	chr9:15970668-16377360	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv429999	chr9:16102066-16389100	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv530933	chr9:16251206-16830845	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv892644	chr9:16275107-16389006	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv530934	chr9:16281246-16779432	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv892645	chr9:16292669-16368732	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv613668	chr9:16310620-16377360	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs914656	TYRP1	cis	parietal	SCAN
rs914656	ZDHHC21	cis	parietal	SCAN

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16312200-16321200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr9:16315400-16335600	Weak transcription	Right Ventricle	heart
3	chr9:16315800-16321200	Weak transcription	NHLF	lung
4	chr9:16316000-16321200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr9:16316400-16321200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:16316600-16321600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr9:16317200-16321200	Weak transcription	Adipose Nuclei	Adipose
8	chr9:16317200-16325400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr9:16317600-16321200	Weak transcription	HSMM	muscle
10	chr9:16318000-16321400	Weak transcription	HSMMtube	muscle
11	chr9:16319200-16321400	Weak transcription	Fetal Lung	lung
12	chr9:16320600-16322000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr9:16320600-16322000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr9:16320600-16322000	Enhancers	Stomach Smooth Muscle	stomach
15	chr9:16320800-16321200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr9:16320800-16321200	Weak transcription	Ovary	ovary
17	chr9:16320800-16321400	Weak transcription	Right Atrium	heart
18	chr9:16320800-16322000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr9:16320800-16323000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr9:16320800-16323000	Weak transcription	Lung	lung
21	chr9:16321000-16322000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr9:16321000-16322000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr9:16321000-16322000	Enhancers	Osteobl	bone

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