Variant report

Variant	rs4642745
Chromosome Location	chr9:17824238-17824239
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:17822817..17825077-chr9:17826697..17828392,2	K562	blood:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10738491	0.86[AFR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10963295	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10963299	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12380227	0.90[ASN][1000 genomes]
rs16923365	0.85[ASN][1000 genomes]
rs16935984	0.85[ASN][1000 genomes]
rs2891113	0.81[ASN][1000 genomes]
rs35911294	0.85[ASN][1000 genomes]
rs3808674	0.81[ASN][1000 genomes]
rs4284123	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4382571	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4415416	0.82[AFR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4430174	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4477127	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4481712	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4531142	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4629969	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4961448	0.90[ASN][1000 genomes]
rs61551917	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6475175	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6475179	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6475180	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7024967	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7027918	0.81[ASN][1000 genomes]
rs73642315	0.81[ASN][1000 genomes]
rs73645334	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73645339	0.90[ASN][1000 genomes]
rs7847592	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7867642	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7871893	0.85[ASN][1000 genomes]
rs7873468	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	nsv824867	chr9:17810486-17828870	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv8422	chr9:17810758-17829560	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv2761507	chr9:17810983-17901307	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv2757321	chr9:17811584-17828437	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv2759675	chr9:17811584-17828437	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv2754695	chr9:17811600-17828400	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17821400-17824400	Weak transcription	Rectal Smooth Muscle	rectum
2	chr9:17823400-17824400	Enhancers	Fetal Heart	heart
3	chr9:17823600-17824600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:17823600-17825800	Enhancers	Fetal Brain Male	brain
5	chr9:17823800-17825600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr9:17824000-17826000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr9:17824200-17824800	Enhancers	Aorta	Aorta
8	chr9:17824200-17825000	Enhancers	Right Atrium	heart
9	chr9:17824200-17825600	Enhancers	Fetal Brain Female	brain

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