Variant report

Variant rs4239300
Chromosome Location chr18:11732957-11732958
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:11727400-11733200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr18:11727600-11733200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr18:11730000-11733200 Weak transcription HMEC breast
4 chr18:11730000-11733200 Weak transcription NHEK skin
5 chr18:11732400-11734800 Weak transcription Right Atrium heart
6 chr18:11732800-11733200 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr18:11732800-11733200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr18:11732800-11733200 Enhancers Fetal Brain Male brain
9 chr18:11732800-11733200 Enhancers A549 lung
10 chr18:11732800-11733400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr18:11732800-11733400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr18:11732800-11733400 Active TSS Brain Dorsolateral Prefrontal Cortex brain
13 chr18:11732800-11733600 Enhancers Primary B cells from peripheral blood blood

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