Variant report

Variant	rs73819921
Chromosome Location	chr3:21440829-21440830
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:21439366..21441034-chr3:21442770..21445274,2	K562	blood:
2	chr3:21439015..21441958-chr3:21447248..21448760,2	K562	blood:
3	chr3:21438293..21442012-chr3:21443506..21445713,3	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs13317408	1.00[EUR][1000 genomes]
rs17008685	1.00[EUR][1000 genomes]
rs17008726	1.00[EUR][1000 genomes]
rs2196440	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56063158	0.87[AFR][1000 genomes]
rs59030260	1.00[EUR][1000 genomes]
rs59308734	1.00[EUR][1000 genomes]
rs60720460	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6781161	1.00[EUR][1000 genomes]
rs73819013	1.00[EUR][1000 genomes]
rs73819018	1.00[EUR][1000 genomes]
rs73819025	1.00[EUR][1000 genomes]
rs73819917	0.87[AFR][1000 genomes]
rs73820004	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73820199	1.00[EUR][1000 genomes]
rs73820939	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73820942	1.00[EUR][1000 genomes]
rs73820944	1.00[EUR][1000 genomes]
rs7619922	1.00[EUR][1000 genomes]
rs9829608	1.00[EUR][1000 genomes]
rs9831471	1.00[EUR][1000 genomes]
rs9854332	1.00[EUR][1000 genomes]
rs9877941	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	nsv834630	chr3:21311619-21491327	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1011516	chr3:21337788-21472093	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1006471	chr3:21385627-21596955	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv534005	chr3:21387588-22003293	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1000828	chr3:21399870-21565580	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv536515	chr3:21399870-21565580	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr3:21433600-21447800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:21435400-21451800	Weak transcription	Aorta	Aorta

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