Variant report

Variant rs10477478
Chromosome Location chr5:111561370-111561371
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:111504800-111586400 Weak transcription Gastric stomach
2 chr5:111538600-111563600 Weak transcription Lung lung
3 chr5:111546600-111561600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr5:111554000-111562800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr5:111554200-111563600 Weak transcription Left Ventricle heart
6 chr5:111554200-111563600 Weak transcription Right Ventricle heart
7 chr5:111554200-111568400 Weak transcription Right Atrium heart
8 chr5:111557000-111563600 Weak transcription Stomach Mucosa stomach
9 chr5:111558200-111561600 Weak transcription H9 Cell Line embryonic stem cell
10 chr5:111558600-111563200 Weak transcription Pancreas Pancrea
11 chr5:111558600-111563400 Weak transcription Placenta Amnion Placenta Amnion
12 chr5:111558600-111584400 Weak transcription Psoas Muscle Psoas
13 chr5:111558800-111591400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr5:111559000-111562200 Weak transcription A549 lung
15 chr5:111559400-111564200 Weak transcription Liver Liver
16 chr5:111560200-111563600 Enhancers Fetal Heart heart
17 chr5:111561000-111562800 Enhancers iPS-18 Cell Line embryonic stem cell
18 chr5:111561200-111562400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived

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