Variant report

Variant rs558523272
Chromosome Location chr16:74870697-74870698
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:74864800-74877200 Weak transcription Fetal Intestine Small intestine
2 chr16:74865000-74870800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr16:74867600-74870800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr16:74868600-74872200 Weak transcription Placenta Placenta
5 chr16:74870000-74872600 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr16:74870600-74870800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
7 chr16:74870600-74877000 Weak transcription Esophagus oesophagus

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