Variant report

Variant	rs6105505
Chromosome Location	chr20:15954877-15954878
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10470063	1.00[EUR][1000 genomes]
rs12624883	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6074981	0.82[AFR][1000 genomes]
rs6080035	0.90[ASN][1000 genomes]
rs6080059	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6110804	1.00[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	nsv869328	chr20:15325423-16213898	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv833929	chr20:15765372-15977337	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv3447866	chr20:15799286-16115291	Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr20:15951600-15955000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr20:15953000-15959800	Weak transcription	Primary B cells from peripheral blood	blood
3	chr20:15953400-15957400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr20:15954600-15955400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr20:15954600-15955400	Enhancers	Adipose Nuclei	Adipose
6	chr20:15954600-15955800	Strong transcription	Primary B cells from cord blood	blood
7	chr20:15954600-15956600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr20:15954600-15959200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr20:15954800-15955200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr20:15954800-15955400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr20:15954800-15955600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr20:15954800-15958800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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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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