Variant report

Variant rs292935
Chromosome Location chr16:72784822-72784823
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:72778600-72791400 Weak transcription Primary B cells from cord blood blood
2 chr16:72780800-72787000 Enhancers Fetal Intestine Small intestine
3 chr16:72782000-72787600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr16:72783200-72787000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr16:72783800-72786600 Weak transcription Primary hematopoietic stem cells blood
6 chr16:72783800-72786800 Weak transcription HepG2 liver
7 chr16:72783800-72810600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr16:72784000-72785200 Enhancers Fetal Heart heart
9 chr16:72784000-72787000 Enhancers Fetal Intestine Large intestine
10 chr16:72784200-72785000 Enhancers Ovary ovary
11 chr16:72784200-72785400 Weak transcription HUES48 Cell Line embryonic stem cell
12 chr16:72784400-72785600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
13 chr16:72784600-72785000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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