Variant report

Variant	rs73744908
Chromosome Location	chr6:55677200-55677201
allele	C/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]
rs55778645	1.00[AMR][1000 genomes]
rs56750083	1.00[AMR][1000 genomes]
rs57385665	1.00[AMR][1000 genomes]
rs58284917	1.00[AMR][1000 genomes]
rs59347412	1.00[AMR][1000 genomes]
rs60070969	1.00[AMR][1000 genomes]
rs6909150	1.00[AMR][1000 genomes]
rs73446194	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73446200	1.00[AMR][1000 genomes]
rs73446201	1.00[AMR][1000 genomes]
rs73448104	1.00[AMR][1000 genomes]
rs73448111	1.00[AMR][1000 genomes]
rs73448135	1.00[AMR][1000 genomes]
rs73744903	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	nsv885910	chr6:55628283-55684300	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 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	chr6:55673600-55678400	Weak transcription	Placenta	Placenta
3	chr6:55673800-55682600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:55676000-55677600	Enhancers	Fetal Lung	lung
5	chr6:55676000-55678000	Enhancers	Fetal Heart	heart
6	chr6:55676600-55683200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr6:55677000-55687800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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