Variant report

Variant	rs35911294
Chromosome Location	chr9:17788973-17788974
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10491540	0.85[EUR][1000 genomes]
rs10738491	0.81[ASN][1000 genomes]
rs10810850	0.88[EUR][1000 genomes]
rs10963249	0.85[EUR][1000 genomes]
rs10963254	0.85[EUR][1000 genomes]
rs10963258	0.86[EUR][1000 genomes]
rs10963261	0.88[EUR][1000 genomes]
rs10963262	0.88[EUR][1000 genomes]
rs10963263	0.88[EUR][1000 genomes]
rs10963264	0.88[EUR][1000 genomes]
rs10963265	0.87[EUR][1000 genomes]
rs10963267	0.87[EUR][1000 genomes]
rs10963268	0.88[EUR][1000 genomes]
rs10963295	0.85[ASN][1000 genomes]
rs10963299	0.85[ASN][1000 genomes]
rs1114790	0.92[EUR][1000 genomes]
rs12005953	0.88[EUR][1000 genomes]
rs12379450	0.88[EUR][1000 genomes]
rs12380227	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13284953	0.85[EUR][1000 genomes]
rs13291415	0.88[EUR][1000 genomes]
rs13291891	0.82[EUR][1000 genomes]
rs16923365	1.00[ASN][1000 genomes]
rs16935984	1.00[ASN][1000 genomes]
rs2891113	0.95[ASN][1000 genomes]
rs34106908	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34609165	0.80[EUR][1000 genomes]
rs36045574	0.84[EUR][1000 genomes]
rs3808674	0.95[ASN][1000 genomes]
rs41305339	0.84[EUR][1000 genomes]
rs4284123	0.95[ASN][1000 genomes]
rs4382571	0.95[ASN][1000 genomes]
rs4415416	0.85[ASN][1000 genomes]
rs4430174	0.95[ASN][1000 genomes]
rs4477127	0.95[ASN][1000 genomes]
rs4481712	0.95[ASN][1000 genomes]
rs4531142	0.95[ASN][1000 genomes]
rs4629969	0.95[ASN][1000 genomes]
rs4642745	0.85[ASN][1000 genomes]
rs4961448	0.80[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs61551917	0.90[ASN][1000 genomes]
rs62549703	0.85[EUR][1000 genomes]
rs6475175	0.81[ASN][1000 genomes]
rs6475179	0.85[ASN][1000 genomes]
rs6475180	0.85[ASN][1000 genomes]
rs7024967	0.81[ASN][1000 genomes]
rs7027918	0.95[ASN][1000 genomes]
rs7044550	0.88[EUR][1000 genomes]
rs73642315	0.95[ASN][1000 genomes]
rs73645334	0.95[ASN][1000 genomes]
rs73645339	0.95[ASN][1000 genomes]
rs7847592	0.85[ASN][1000 genomes]
rs7867642	0.85[ASN][1000 genomes]
rs7871893	1.00[ASN][1000 genomes]
rs7873468	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892675	chr9:17694823-17790526	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv613706	chr9:17718918-18090934	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv613707	chr9:17720175-18070475	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv613708	chr9:17720175-18072085	Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1034673	chr9:17739006-17916606	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1023089	chr9:17748811-17919574	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17784800-17799400	Weak transcription	Hela-S3	cervix
2	chr9:17787000-17800400	Weak transcription	Fetal Brain Female	brain
3	chr9:17787200-17791000	Weak transcription	Fetal Brain Male	brain
4	chr9:17788600-17805400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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