Variant report

Variant rs13332329
Chromosome Location chr16:79829011-79829012
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:79814000-79839600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr16:79823600-79829800 Weak transcription Esophagus oesophagus
3 chr16:79824200-79829400 Enhancers Fetal Stomach stomach
4 chr16:79827000-79829600 Enhancers Ovary ovary
5 chr16:79827600-79830800 Weak transcription Fetal Muscle Leg muscle
6 chr16:79827600-79831200 Enhancers Fetal Lung lung
7 chr16:79827800-79830000 Enhancers NHEK skin
8 chr16:79828000-79829600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr16:79828600-79829200 Enhancers Aorta Aorta
10 chr16:79829000-79829200 Enhancers Brain Inferior Temporal Lobe brain
11 chr16:79829000-79829200 Enhancers Fetal Brain Male brain
12 chr16:79829000-79829400 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr16:79829000-79829400 Enhancers Cortex derived primary cultured neurospheres brain
14 chr16:79829000-79829600 Enhancers ES-I3 Cell Line embryonic stem cell
15 chr16:79829000-79830000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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