Variant report

Variant rs552731619
Chromosome Location chr3:141819372-141819373
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:141761800-141819600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr3:141763000-141820000 Weak transcription Pancreas Pancrea
3 chr3:141763000-141824200 Weak transcription Aorta Aorta
4 chr3:141764000-141825600 Weak transcription Primary T cells from cord blood blood
5 chr3:141795400-141835800 Weak transcription Primary Natural Killer cells fromperipheralblood blood
6 chr3:141797600-141819600 Weak transcription Fetal Muscle Leg muscle
7 chr3:141797600-141823600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
8 chr3:141804000-141820800 Weak transcription Left Ventricle heart
9 chr3:141815400-141821000 Genic enhancers Fetal Thymus thymus
10 chr3:141817400-141819800 Enhancers K562 blood
11 chr3:141817800-141819600 Enhancers Thymus Thymus
12 chr3:141818200-141822600 Enhancers Dnd41 blood
13 chr3:141818200-141830600 Weak transcription Fetal Intestine Small intestine
14 chr3:141818200-141835800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr3:141819000-141819800 Strong transcription Fetal Intestine Large intestine
16 chr3:141819200-141827000 Weak transcription Primary hematopoietic stem cells short term culture blood

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