Variant report

Variant	rs73513043
Chromosome Location	chr9:94327045-94327046
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:94314127..94316107-chr9:94326868..94329032,2	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10512214	1.00[AMR][1000 genomes]
rs11998997	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12001172	1.00[AMR][1000 genomes]
rs12001678	1.00[AMR][1000 genomes]
rs12001758	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12003706	1.00[AMR][1000 genomes]
rs12003741	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16907588	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16907602	1.00[AMR][1000 genomes]
rs35764413	1.00[AMR][1000 genomes]
rs4381076	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56091954	1.00[AMR][1000 genomes]
rs56227711	1.00[AMR][1000 genomes]
rs57006470	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57412003	1.00[AMR][1000 genomes]
rs59365117	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60009660	1.00[AMR][1000 genomes]
rs60217100	1.00[AMR][1000 genomes]
rs60341050	1.00[AMR][1000 genomes]
rs61094317	1.00[AMR][1000 genomes]
rs6479372	1.00[AMR][1000 genomes]
rs6479373	1.00[AMR][1000 genomes]
rs7026091	1.00[AMR][1000 genomes]
rs73494674	1.00[AMR][1000 genomes]
rs73496706	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73496717	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73496726	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73496729	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73496737	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73496741	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73496743	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73513020	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73513032	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73513061	1.00[AMR][1000 genomes]
rs73513068	1.00[AMR][1000 genomes]
rs73515039	1.00[AMR][1000 genomes]
rs73521420	1.00[AMR][1000 genomes]
rs73521430	1.00[AMR][1000 genomes]
rs7873653	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3332537	chr9:94298446-94327291	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94320400-94333800	Weak transcription	Stomach Smooth Muscle	stomach
2	chr9:94326000-94327600	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr9:94326000-94327800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr9:94326000-94327800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr9:94326200-94327200	Enhancers	H1 Cell Line	embryonic stem cell
6	chr9:94326200-94327400	Enhancers	H9 Cell Line	embryonic stem cell
7	chr9:94326200-94327400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:94326200-94327600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr9:94326200-94327600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr9:94326200-94327800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr9:94326400-94330000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr9:94327000-94327200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr9:94327000-94327400	Enhancers	iPS-20b Cell Line	embryonic stem cell

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