Variant report

Variant	rs6076233
Chromosome Location	chr20:24494024-24494025
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13041310	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1555892	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2386954	0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2386956	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4283490	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6036832	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6049750	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6049755	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6049757	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6049758	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6049759	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6049760	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6049765	0.83[EUR][1000 genomes]
rs6049768	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6049771	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6049775	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6076235	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6114752	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6114757	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6114760	0.81[EUR][1000 genomes]
rs6132738	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6132742	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6132743	0.86[EUR][1000 genomes]
rs6138310	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6138316	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv9793	chr20:23939613-24734850	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1058146	chr20:24210196-24531087	Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv178771	chr20:24492791-24498267	Enhancers Weak transcription Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24475600-24495600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr20:24481600-24504200	Weak transcription	Fetal Brain Male	brain
3	chr20:24488600-24498800	Weak transcription	Brain Hippocampus Middle	brain
4	chr20:24491400-24508600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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