Variant report

Variant rs2904214
Chromosome Location chr16:74869794-74869795
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:5 , 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 chr16:74866000-74870000 Weak transcription Esophagus oesophagus
4 chr16:74867600-74870800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr16:74868600-74872200 Weak transcription Placenta Placenta

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