Variant report

Variant	rs73582277
Chromosome Location	chr6:147266533-147266534
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs6925007	1.00[EUR][1000 genomes]
rs6932987	1.00[EUR][1000 genomes]
rs73584145	1.00[EUR][1000 genomes]
rs73584171	1.00[EUR][1000 genomes]
rs7738861	1.00[EUR][1000 genomes]
rs7742290	1.00[EUR][1000 genomes]
rs7747577	1.00[EUR][1000 genomes]
rs7770138	1.00[EUR][1000 genomes]
rs7771739	1.00[EUR][1000 genomes]
rs7771849	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	nsv830838	chr6:147090745-147274669	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	esv2760996	chr6:147229457-147269633	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv1846046	chr6:147258908-147271295	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147265600-147266800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:147265600-147276600	Weak transcription	Pancreas	Pancrea
3	chr6:147266200-147268000	Enhancers	HepG2	liver
4	chr6:147266400-147268800	Enhancers	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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