Variant report

Variant	rs55778645
Chromosome Location	chr6:55685882-55685883
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs4576248	1.00[AMR][1000 genomes]
rs56750083	1.00[AMR][1000 genomes]
rs57385665	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58284917	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59347412	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60070969	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6909150	1.00[AMR][1000 genomes]
rs73446194	1.00[AMR][1000 genomes]
rs73446200	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73446201	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73448104	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73448111	1.00[AMR][1000 genomes]
rs73448135	1.00[AMR][1000 genomes]
rs73744903	1.00[AMR][1000 genomes]
rs73744908	1.00[AMR][1000 genomes]
rs7766232	1.00[AMR][1000 genomes]
rs7767545	1.00[AMR][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	nsv1034037	chr6:55222409-56069600	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv2752670	chr6:55614978-55781605	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv1032684	chr6:55680473-55766876	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55670800-55688200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr6:55677000-55687800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr6:55681800-55686600	Weak transcription	Fetal Heart	heart
4	chr6:55683200-55688000	Weak transcription	Fetal Lung	lung
5	chr6:55683600-55689200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:55683800-55687600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr6:55684000-55692000	Weak transcription	Fetal Brain Male	brain
8	chr6:55684400-55687800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:55685000-55687600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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