Variant report

Variant	rs73654349
Chromosome Location	chr9:96673265-96673266
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:96673253..96675820-chr9:96696121..96697775,2	MCF-7	breast:
2	chr9:96672827..96673633-chr9:96725329..96725969,2	K562	blood:
3	chr9:96672307..96674659-chr9:96674694..96676957,2	MCF-7	breast:
4	chr9:96669102..96671238-chr9:96671311..96673716,2	MCF-7	breast:
5	chr9:96670566..96673928-chr9:96676412..96679551,4	K562	blood:
6	chr9:96669941..96671466-chr9:96672760..96674877,2	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs3909255	1.00[EUR][1000 genomes]
rs57293846	1.00[EUR][1000 genomes]
rs57474922	1.00[EUR][1000 genomes]
rs57992049	1.00[EUR][1000 genomes]
rs58184281	1.00[EUR][1000 genomes]
rs60296005	1.00[EUR][1000 genomes]
rs60574743	1.00[EUR][1000 genomes]
rs60859572	1.00[EUR][1000 genomes]
rs61209800	1.00[EUR][1000 genomes]
rs7028775	1.00[EUR][1000 genomes]
rs7036040	1.00[EUR][1000 genomes]
rs7042611	1.00[EUR][1000 genomes]
rs73516288	1.00[EUR][1000 genomes]
rs73517134	1.00[EUR][1000 genomes]
rs73517146	1.00[EUR][1000 genomes]
rs73517153	1.00[EUR][1000 genomes]
rs73518256	1.00[EUR][1000 genomes]
rs73518290	1.00[EUR][1000 genomes]
rs73653403	1.00[EUR][1000 genomes]
rs73653404	1.00[EUR][1000 genomes]
rs73653406	1.00[EUR][1000 genomes]
rs73653435	1.00[EUR][1000 genomes]
rs73653436	1.00[EUR][1000 genomes]
rs73654365	1.00[EUR][1000 genomes]
rs73654369	1.00[EUR][1000 genomes]
rs73654372	1.00[EUR][1000 genomes]
rs73654793	1.00[EUR][1000 genomes]
rs73654794	1.00[EUR][1000 genomes]
rs73654796	1.00[EUR][1000 genomes]
rs7853152	1.00[EUR][1000 genomes]
rs7874412	1.00[EUR][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	nsv893589	chr9:96624645-96884544	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1053137	chr9:96644876-96683214	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv1046904	chr9:96647940-96689327	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv1035418	chr9:96647940-96711409	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	esv1801607	chr9:96657324-96683214	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv1042043	chr9:96657324-96689327	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96665400-96674400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:96666000-96674600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:96671000-96675400	Bivalent Enhancer	Fetal Stomach	stomach
4	chr9:96671400-96673400	Enhancers	Stomach Smooth Muscle	stomach
5	chr9:96671400-96674400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr9:96671400-96679600	Weak transcription	Gastric	stomach
7	chr9:96671800-96674800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr9:96672000-96674800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr9:96673200-96673800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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