Variant report

Variant rs189138131
Chromosome Location chr3:141824315-141824316
allele C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:141764000-141825600 Weak transcription Primary T cells from cord blood blood
2 chr3:141795400-141835800 Weak transcription Primary Natural Killer cells fromperipheralblood blood
3 chr3:141818200-141830600 Weak transcription Fetal Intestine Small intestine
4 chr3:141818200-141835800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr3:141819200-141827000 Weak transcription Primary hematopoietic stem cells short term culture blood
6 chr3:141821200-141827000 Weak transcription Thymus Thymus
7 chr3:141822200-141825400 Weak transcription Fetal Thymus thymus
8 chr3:141823600-141825400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr3:141823600-141832000 Enhancers Dnd41 blood
10 chr3:141823800-141824400 Enhancers HepG2 liver
11 chr3:141823800-141825800 Enhancers Pancreatic Islets Pancreatic Islet
12 chr3:141824000-141826000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr3:141824200-141824400 Enhancers Aorta Aorta
14 chr3:141824200-141824400 Enhancers Fetal Intestine Large intestine

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