Variant report

Variant	rs56215630
Chromosome Location	chr6:133895738-133895739
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11757578	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2327358	0.99[EUR][1000 genomes]
rs58342792	1.00[EUR][1000 genomes]
rs6911166	1.00[EUR][1000 genomes]
rs6911916	1.00[EUR][1000 genomes]
rs6912223	1.00[EUR][1000 genomes]
rs6912460	1.00[EUR][1000 genomes]
rs7757204	0.92[EUR][1000 genomes]
rs9321406	0.99[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	nsv886682	chr6:133892208-133943732	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133893800-133898400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr6:133894800-133896000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:133895200-133895800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr6:133895200-133895800	Enhancers	Osteobl	bone
5	chr6:133895400-133895800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:133895600-133908000	Weak transcription	NHDF-Ad	bronchial

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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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