Variant report

Variant	rs73845119
Chromosome Location	chr4:121216492-121216493
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10006083	1.00[AMR][1000 genomes]
rs10028188	1.00[AMR][1000 genomes]
rs11930109	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17012236	0.83[AMR][1000 genomes]
rs17012768	0.85[AFR][1000 genomes]
rs28679486	1.00[AMR][1000 genomes]
rs34532006	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34864233	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59042587	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60577273	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60782621	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73842902	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73845103	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73845105	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73845106	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73845116	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73845134	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73845136	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73845137	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73845139	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73845140	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73845151	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007641	chr4:120884220-121555889	Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv537234	chr4:120884220-121555889	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv595333	chr4:121093248-121440368	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1005240	chr4:121093285-121420997	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv879852	chr4:121108734-121768496	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121214600-121218400	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr4:121215400-121217800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr4:121215400-121218400	Weak transcription	Osteobl	bone
4	chr4:121215800-121218000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr4:121216400-121217000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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