Variant report

Variant	rs534043
Chromosome Location	chr7:100312724-100312725
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:100305231..100306842-chr7:100311129..100313702,2	K562	blood:
2	chr7:100311308..100312814-chr7:100315076..100317499,2	K562	blood:
3	chr7:100308383..100310094-chr7:100311797..100313308,2	MCF-7	breast:
4	chr7:100301529..100304641-chr7:100311739..100314929,3	K562	blood:
5	chr7:100302126..100304908-chr7:100310988..100312832,3	MCF-7	breast:
6	chr7:100311164..100312839-chr7:100313147..100315686,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000172336	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1734907	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs221770	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs221774	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs221778	0.90[EUR][1000 genomes]
rs221779	0.80[EUR][1000 genomes]
rs221780	0.93[ASN][1000 genomes]
rs221781	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs221783	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs221784	1.00[ASN][1000 genomes]
rs221786	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs221789	0.87[ASN][1000 genomes]
rs221792	1.00[ASN][1000 genomes]
rs221793	0.81[EUR][1000 genomes]
rs221794	0.96[ASN][1000 genomes]
rs221796	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs221797	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs221798	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs221800	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs221803	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2432929	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4727462	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs492430	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs506597	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs564449	0.96[EUR][1000 genomes];0.93[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	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
2	nsv888779	chr7:100014711-100313420	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	321 gene(s)	inside rSNPs	diseases
3	nsv888785	chr7:100141861-100313420	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
4	nsv888786	chr7:100159567-100313420	Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
5	nsv831072	chr7:100162503-100362835	Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
6	nsv888791	chr7:100221867-100371114	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
7	nsv607933	chr7:100240191-100365613	Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
8	nsv470381	chr7:100240191-100431980	Strong transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
9	nsv8184	chr7:100240737-100345945	Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
10	nsv888792	chr7:100252918-100329189	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
11	esv1804951	chr7:100275135-100374093	Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs534043	GIGYF1	cis	Nerve Tibial	GTEx

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100305000-100318000	Weak transcription	Right Atrium	heart
2	chr7:100305200-100313200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr7:100305200-100313400	Weak transcription	Brain Germinal Matrix	brain
4	chr7:100305200-100315000	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr7:100305200-100318400	Weak transcription	Gastric	stomach
6	chr7:100305400-100313000	Weak transcription	NH-A	brain
7	chr7:100306000-100313200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr7:100306200-100314400	Weak transcription	Lung	lung
9	chr7:100306400-100313200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr7:100306800-100315400	Weak transcription	Placenta	Placenta
11	chr7:100306800-100315600	Weak transcription	HepG2	liver
12	chr7:100312600-100314200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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