Variant report

Variant rs7234732
Chromosome Location chr18:43904903-43904904
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:43899800-43905000 Enhancers HMEC breast
2 chr18:43901200-43905600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr18:43902600-43905400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr18:43902800-43905000 Enhancers NHEK skin
5 chr18:43902800-43905800 Weak transcription Esophagus oesophagus
6 chr18:43902800-43906200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr18:43903200-43909800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr18:43903200-43909800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
9 chr18:43903600-43905000 Enhancers Primary monocytes fromperipheralblood blood
10 chr18:43904200-43905000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr18:43904200-43905000 Enhancers Lung lung
12 chr18:43904600-43905400 Enhancers Hela-S3 cervix
13 chr18:43904600-43905600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr18:43904800-43905000 Enhancers Dnd41 blood
15 chr18:43904800-43905000 Enhancers Monocytes-CD14+_RO01746 blood
16 chr18:43904800-43905800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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