Variant report

Variant	rs73330543
Chromosome Location	chr14:81106965-81106966
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	chr14:81105972..81108126-chr14:81297370..81299564,2	K562	blood:

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10133617	1.00[EUR][1000 genomes]
rs10136245	1.00[EUR][1000 genomes]
rs10137925	1.00[EUR][1000 genomes]
rs10140445	1.00[EUR][1000 genomes]
rs10144134	1.00[EUR][1000 genomes]
rs10150034	1.00[EUR][1000 genomes]
rs10151027	1.00[EUR][1000 genomes]
rs10151108	1.00[EUR][1000 genomes]
rs10220319	1.00[EUR][1000 genomes]
rs1375628	1.00[EUR][1000 genomes]
rs17110847	1.00[EUR][1000 genomes]
rs17111025	1.00[EUR][1000 genomes]
rs2197983	1.00[EUR][1000 genomes]
rs28529404	1.00[EUR][1000 genomes]
rs28650423	1.00[EUR][1000 genomes]
rs327432	1.00[EUR][1000 genomes]
rs327437	1.00[EUR][1000 genomes]
rs56933416	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57834417	1.00[EUR][1000 genomes]
rs58268321	1.00[EUR][1000 genomes]
rs58594627	1.00[EUR][1000 genomes]
rs58595334	1.00[EUR][1000 genomes]
rs60207137	1.00[EUR][1000 genomes]
rs61435414	1.00[EUR][1000 genomes]
rs73326644	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73326672	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73328649	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73328655	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73328682	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73330508	1.00[EUR][1000 genomes]
rs73330519	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73330520	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73332696	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73334792	1.00[EUR][1000 genomes]
rs73336577	1.00[EUR][1000 genomes]
rs73336590	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73336591	1.00[EUR][1000 genomes]
rs73336597	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73338156	1.00[EUR][1000 genomes]
rs73338189	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73338199	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73338970	1.00[EUR][1000 genomes]
rs73338973	1.00[EUR][1000 genomes]
rs73340105	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73340107	1.00[EUR][1000 genomes]
rs73340171	1.00[EUR][1000 genomes]
rs73340517	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73340530	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73342506	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73342522	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73342549	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73342552	1.00[EUR][1000 genomes]
rs73342554	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74064297	1.00[EUR][1000 genomes]
rs8020092	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv565290	chr14:81085129-81230117	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81083400-81109400	Weak transcription	Dnd41	blood
2	chr14:81099000-81109600	Weak transcription	Thymus	Thymus
3	chr14:81105400-81112800	Weak transcription	HSMM	muscle
4	chr14:81105800-81107000	Enhancers	A549	lung
5	chr14:81105800-81107200	Enhancers	HUVEC	blood vessel
6	chr14:81105800-81112000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr14:81106200-81112400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr14:81106200-81135400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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