Variant report

Variant rs11855487
Chromosome Location chr15:39924129-39924130
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:39916400-39937800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr15:39917600-39926200 Weak transcription Esophagus oesophagus
3 chr15:39920000-39924400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr15:39920200-39924400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr15:39920600-39924200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr15:39920800-39924400 Enhancers NHEK skin
7 chr15:39920800-39925200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
8 chr15:39921200-39924400 Enhancers Fetal Heart heart
9 chr15:39921400-39924400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr15:39921400-39926200 Weak transcription Pancreas Pancrea
11 chr15:39921400-39937600 Weak transcription Psoas Muscle Psoas
12 chr15:39923400-39924400 Enhancers NH-A brain
13 chr15:39923600-39925400 Enhancers Primary T helper 17 cells PMA-I stimulated --
14 chr15:39923800-39926200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr15:39923800-39939600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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