Variant report

Variant	rs7979037
Chromosome Location	chr12:123155565-123155566
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123153000-123157200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr12:123154200-123155800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr12:123154400-123155800	Weak transcription	HepG2	liver
4	chr12:123154800-123156600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr12:123154800-123163200	Weak transcription	Osteobl	bone
6	chr12:123155200-123161800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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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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