Variant report

Variant	rs13038938
Chromosome Location	chr20:24601943-24601944
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs13040375	0.90[GIH][hapmap];0.92[MEX][hapmap];0.80[MKK][hapmap]
rs6083563	0.85[AMR][1000 genomes];0.85[EUR][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	esv3332519	chr20:24535099-24815615	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr20:24584400-24612600	Weak transcription	Aorta	Aorta
2	chr20:24591200-24609200	Weak transcription	Brain Anterior Caudate	brain
3	chr20:24594400-24608400	Weak transcription	Spleen	Spleen
4	chr20:24600000-24609600	Weak transcription	Brain Angular Gyrus	brain
5	chr20:24600200-24608200	Weak transcription	Brain Hippocampus Middle	brain
6	chr20:24600600-24608000	Weak transcription	Right Atrium	heart
7	chr20:24600600-24608400	Weak transcription	Fetal Heart	heart
8	chr20:24600600-24608800	Weak transcription	Thymus	Thymus
9	chr20:24600800-24602000	Weak transcription	Fetal Lung	lung
10	chr20:24601200-24602400	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr20:24601400-24602200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr20:24601800-24602400	Enhancers	Liver	Liver

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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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