Variant report

Variant rs59159077
Chromosome Location chr2:182629997-182629998
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:5 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:182616800-182631000 Weak transcription Placenta Amnion Placenta Amnion
2 chr2:182627800-182630200 Enhancers HepG2 liver
3 chr2:182629600-182630400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr2:182629600-182630800 Weak transcription Fetal Intestine Small intestine
5 chr2:182629800-182630800 Weak transcription Stomach Mucosa stomach

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