Variant report

Variant rs11787180
Chromosome Location chr8:104672253-104672254
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:104654200-104706400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr8:104663400-104682000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr8:104663600-104672400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr8:104663600-104687600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr8:104664800-104682000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr8:104665400-104683000 Weak transcription Pancreatic Islets Pancreatic Islet
7 chr8:104665800-104674400 Weak transcription HUES6 Cell Line embryonic stem cell
8 chr8:104666800-104680400 Weak transcription HUES64 Cell Line embryonic stem cell
9 chr8:104669200-104681200 Weak transcription iPS-20b Cell Line embryonic stem cell
10 chr8:104669600-104674800 Weak transcription HUES48 Cell Line embryonic stem cell
11 chr8:104670400-104672800 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr8:104671600-104672800 Strong transcription iPS-15b Cell Line embryonic stem cell
13 chr8:104672000-104672400 Weak transcription Fetal Adrenal Gland Adrenal Gland
14 chr8:104672000-104672600 Strong transcription H1 Cell Line embryonic stem cell
15 chr8:104672200-104672800 Strong transcription H9 Cell Line embryonic stem cell

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