Variant report

Variant	rs73324268
Chromosome Location	chr8:112440910-112440911
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs16882021	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56719443	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59523937	1.00[AMR][1000 genomes]
rs6999561	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7010597	1.00[AMR][1000 genomes]
rs73324253	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73324254	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73324261	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73324287	1.00[AMR][1000 genomes]
rs73324289	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73324292	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73324297	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73326018	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73326055	1.00[AMR][1000 genomes]
rs73327916	1.00[AMR][1000 genomes]
rs73327944	1.00[AMR][1000 genomes]
rs73327951	1.00[AMR][1000 genomes]
rs73329965	1.00[AMR][1000 genomes]
rs73329983	1.00[AMR][1000 genomes]
rs73329986	1.00[AMR][1000 genomes]
rs73332262	1.00[AMR][1000 genomes]
rs73341404	1.00[AMR][1000 genomes]
rs7821717	1.00[AMR][1000 genomes]
rs7842965	1.00[AMR][1000 genomes]
rs7843018	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891311	chr8:112088322-112604086	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv465763	chr8:112325064-112712038	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv611902	chr8:112325064-112712038	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1031144	chr8:112327722-112558646	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1027249	chr8:112327722-112711706	Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv539721	chr8:112327722-112711706	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv891313	chr8:112359706-112548351	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1028518	chr8:112382141-112459890	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1026097	chr8:112382141-112714042	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1017231	chr8:112393019-112711706	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv433251	chr8:112400841-112455664	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv916709	chr8:112439641-112697491	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:112440800-112441000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
2	chr8:112440800-112441800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell

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