Variant report

Variant	rs77467007
Chromosome Location	chr8:49659327-49659328
allele	-/TT
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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	esv2761425	chr8:49658066-49669601	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv368707	chr8:49659328-49659328	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	n/a	n/a
3	esv1918148	chr8:49659328-49659330	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	n/a	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49648600-49661000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr8:49649800-49660200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr8:49656800-49662400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:49659200-49661400	Enhancers	Fetal Lung	lung

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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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