Variant report

Variant	rs567641300
Chromosome Location	chr6:24145658-24145659
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029930	chr6:23481989-24289948	Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv3367849	chr6:24144473-24146521	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24127600-24146800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr6:24141600-24145800	Weak transcription	Brain Anterior Caudate	brain
3	chr6:24142000-24145800	Weak transcription	Brain Angular Gyrus	brain
4	chr6:24142000-24145800	Weak transcription	Brain Germinal Matrix	brain
5	chr6:24142000-24148000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr6:24142000-24149800	Weak transcription	Fetal Brain Male	brain
7	chr6:24142200-24147800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr6:24144800-24148400	Weak transcription	Fetal Brain Female	brain
9	chr6:24145600-24146400	Flanking Active TSS	HepG2	liver
10	chr6:24145600-24146600	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr6:24145600-24149600	Enhancers	Cortex derived primary cultured neurospheres	brain

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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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