Variant report

Variant	rs6043660
Chromosome Location	chr20:15967533-15967534
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11700271	0.97[EUR][1000 genomes]
rs2105203	0.86[ASN][1000 genomes]
rs41275442	0.97[EUR][1000 genomes]
rs61077479	0.91[ASN][1000 genomes]
rs61488901	0.91[ASN][1000 genomes]
rs62194199	0.90[ASN][1000 genomes]
rs62194202	0.90[ASN][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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6043660	MACROD2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:15959000-15985400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr20:15960200-15972600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr20:15960400-15968000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr20:15964400-15967600	Active TSS	GM12878-XiMat	blood
5	chr20:15967200-15968000	Enhancers	Primary B cells from peripheral blood	blood
6	chr20:15967200-15968200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr20:15967200-15968400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr20:15967400-15967800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr20:15967400-15967800	Genic enhancers	Primary B cells from cord blood	blood

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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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