Variant report

Variant	rs6023341
Chromosome Location	chr20:53139065-53139066
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs17326001	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17326260	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs2426522	0.85[EUR][1000 genomes]
rs2426529	0.92[EUR][1000 genomes]
rs2426530	0.93[EUR][1000 genomes]
rs2426536	0.82[EUR][1000 genomes]
rs6014046	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs6023342	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6023344	0.93[EUR][1000 genomes]
rs6023346	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs6098064	0.81[EUR][1000 genomes]
rs62214422	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs66842421	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs67854575	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs726770	0.92[EUR][1000 genomes]
rs7272302	0.90[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv586224	chr20:52474850-53279490	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	338 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	chr20:53120800-53148800	Weak transcription	Left Ventricle	heart
2	chr20:53128600-53142800	Weak transcription	Psoas Muscle	Psoas
3	chr20:53129600-53149200	Weak transcription	Aorta	Aorta
4	chr20:53131400-53140400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr20:53131400-53140800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr20:53132400-53140600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr20:53132400-53142000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr20:53132600-53140400	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr20:53133200-53140800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr20:53133800-53140400	Weak transcription	Fetal Brain Female	brain
11	chr20:53137000-53142200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr20:53137600-53142200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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Input of quick search could be:

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

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