Variant report

Variant	rs73830239
Chromosome Location	chr4:79952157-79952158
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:79944609..79947579-chr4:79951684..79954668,2	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs57602269	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57941709	0.83[AFR][1000 genomes]
rs58561548	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73828203	1.00[AFR][1000 genomes]
rs73828204	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73828229	1.00[AMR][1000 genomes]
rs73830208	1.00[AMR][1000 genomes]
rs73830226	1.00[AMR][1000 genomes]
rs73830240	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73830242	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73830243	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73830246	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73830250	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73830251	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73830252	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73830253	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73830254	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73830258	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73830262	1.00[AMR][1000 genomes]
rs73830269	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73830271	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73830272	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73830274	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73830280	1.00[AFR][1000 genomes]
rs73830281	1.00[AFR][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	nsv829979	chr4:79819168-80019159	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1000907	chr4:79838948-80224764	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv879505	chr4:79887043-80293046	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv3448470	chr4:79898340-80026510	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv432614	chr4:79910989-79993822	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1010833	chr4:79945299-79964080	Enhancers Weak transcription	Chromatin interactive region	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	chr4:79951800-79952200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr4:79952000-79952600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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