Variant report

Variant rs2798317
Chromosome Location chr9:115399064-115399065
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:115379000-115410200 Weak transcription HSMMtube muscle
2 chr9:115381000-115402800 Weak transcription Primary T cells from cord blood blood
3 chr9:115381200-115400600 Weak transcription Fetal Intestine Small intestine
4 chr9:115381200-115401600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr9:115381200-115401600 Weak transcription Dnd41 blood
6 chr9:115383000-115399800 Weak transcription Gastric stomach
7 chr9:115383600-115401400 Weak transcription Primary hematopoietic stem cells short term culture blood
8 chr9:115387600-115401400 Weak transcription Esophagus oesophagus
9 chr9:115388000-115401400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr9:115392400-115401400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr9:115392400-115401400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr9:115392400-115415600 Weak transcription iPS-18 Cell Line embryonic stem cell
13 chr9:115392400-115421600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
14 chr9:115392600-115401200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
15 chr9:115392600-115401400 Weak transcription H1 Cell Line embryonic stem cell
16 chr9:115392600-115401600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
17 chr9:115392600-115401600 Weak transcription Fetal Stomach stomach
18 chr9:115392600-115410400 Weak transcription Ovary ovary
19 chr9:115394200-115401400 Weak transcription Primary B cells from cord blood blood
20 chr9:115397800-115408000 Weak transcription HepG2 liver
21 chr9:115398200-115401400 Weak transcription Fetal Intestine Large intestine
22 chr9:115398200-115401800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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