Variant report

Variant	rs6138316
Chromosome Location	chr20:24517375-24517376
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1555892	0.83[EUR][1000 genomes]
rs2386956	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6036832	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6049755	0.86[EUR][1000 genomes]
rs6049757	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6049758	0.86[EUR][1000 genomes]
rs6049759	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6049760	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6049765	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6049768	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6049771	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6049775	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6076233	0.81[EUR][1000 genomes]
rs6076235	0.85[EUR][1000 genomes]
rs6114752	0.80[EUR][1000 genomes]
rs6114757	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6114768	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6132742	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6132743	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][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	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

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24504000-24525800	Weak transcription	Aorta	Aorta
2	chr20:24508200-24523800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr20:24510800-24518000	Weak transcription	Gastric	stomach
4	chr20:24510800-24525200	Weak transcription	Left Ventricle	heart
5	chr20:24514800-24525800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr20:24515400-24517400	Enhancers	Brain Angular Gyrus	brain
7	chr20:24515800-24524800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr20:24516800-24523000	Weak transcription	Brain Hippocampus Middle	brain
9	chr20:24516800-24524200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr20:24517000-24523800	Weak transcription	Brain Cingulate Gyrus	brain
11	chr20:24517200-24526600	Weak transcription	Brain Substantia Nigra	brain
12	chr20:24517200-24526800	Weak transcription	Brain Inferior Temporal Lobe	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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