Variant report

Variant	rs10115864
Chromosome Location	chr9:97147026-97147027
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10122398	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10125744	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10283669	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1061835	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10993191	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10993194	0.81[ASN][1000 genomes]
rs12338572	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12341403	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12343123	0.85[ASN][1000 genomes]
rs28567659	0.82[EUR][1000 genomes]
rs28704121	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28802403	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55936246	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55962682	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56165201	0.82[EUR][1000 genomes]
rs56404236	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6479541	0.87[ASN][1000 genomes]
rs7024607	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7025878	0.88[ASN][1000 genomes]
rs7030326	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7030967	0.85[ASN][1000 genomes]
rs7036474	0.81[ASN][1000 genomes]
rs7040774	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7045712	0.83[ASN][1000 genomes]
rs7046779	0.83[ASN][1000 genomes]
rs7856786	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7859955	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9632920	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[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	nsv893592	chr9:96973995-97295269	Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1046906	chr9:96999227-97239809	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	esv2761545	chr9:97025298-97356950	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv1041195	chr9:97054795-97402378	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv982324	chr9:97139062-97200156	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs10115864	RP11-307E17.8	cis	Esophagus Muscularis	GTEx
rs10115864	HIATL1	cis	Esophagus Mucosa	GTEx
rs10115864	HIATL1	cis	Nerve Tibial	GTEx
rs10115864	HIATL1	cis	Thyroid	GTEx
rs10115864	HIATL1	cis	lung	GTEx
rs10115864	HIATL1	cis	Adipose Subcutaneous	GTEx
rs10115864	HIATL1	cis	Skin Sun Exposed Lower leg	GTEx
rs10115864	HIATL1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97137800-97153000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr9:97138000-97149000	Weak transcription	Fetal Intestine Small	intestine
3	chr9:97138200-97162400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr9:97138400-97152800	Weak transcription	Primary B cells from peripheral blood	blood
5	chr9:97138800-97152800	Weak transcription	Hela-S3	cervix
6	chr9:97138800-97168600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr9:97139000-97159600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr9:97142600-97147600	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr9:97146400-97148400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr9:97146600-97147200	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr9:97146600-97147800	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr9:97147000-97147200	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr9:97147000-97159600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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