Variant report

Variant rs538912054
Chromosome Location chr14:24474941-24474942
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:24458800-24476000 Weak transcription Fetal Intestine Small intestine
2 chr14:24459000-24475200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chr14:24459200-24476000 Weak transcription Liver Liver
4 chr14:24459400-24475800 Weak transcription Rectal Mucosa Donor 29 rectum
5 chr14:24470800-24475000 Weak transcription Primary monocytes fromperipheralblood blood
6 chr14:24471200-24475000 Weak transcription Primary B cells from peripheral blood blood
7 chr14:24471200-24475000 Weak transcription Monocytes-CD14+_RO01746 blood
8 chr14:24472800-24476000 Weak transcription Pancreas Pancrea
9 chr14:24474000-24475800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr14:24474800-24475000 Enhancers Primary B cells from cord blood blood
11 chr14:24474800-24475000 Enhancers Fetal Brain Female brain
12 chr14:24474800-24475200 Enhancers Primary T helper naive cells from peripheral blood blood
13 chr14:24474800-24475400 Enhancers Dnd41 blood

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