Variant report

Variant rs7042335
Chromosome Location chr9:95122547-95122548
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:25 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:95116800-95127600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:95116800-95128600 Weak transcription Dnd41 blood
3 chr9:95117000-95134800 Weak transcription Ovary ovary
4 chr9:95118000-95135000 Weak transcription Monocytes-CD14+_RO01746 blood
5 chr9:95120000-95131400 Weak transcription Thymus Thymus
6 chr9:95120400-95130600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
7 chr9:95120600-95128000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr9:95120600-95128600 Weak transcription K562 blood
9 chr9:95121600-95122800 Enhancers Fetal Stomach stomach
10 chr9:95121800-95122600 Enhancers Fetal Intestine Large intestine
11 chr9:95121800-95122800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr9:95121800-95122800 Enhancers Primary hematopoietic stem cells blood
13 chr9:95121800-95122800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr9:95121800-95122800 Enhancers Colon Smooth Muscle Colon
15 chr9:95121800-95122800 Enhancers Fetal Heart heart
16 chr9:95121800-95122800 Enhancers Fetal Thymus thymus
17 chr9:95121800-95122800 Enhancers GM12878-XiMat blood
18 chr9:95122000-95122800 Enhancers Primary B cells from peripheral blood blood
19 chr9:95122200-95122800 Enhancers Rectal Smooth Muscle rectum
20 chr9:95122200-95138600 Weak transcription Aorta Aorta
21 chr9:95122400-95122600 Enhancers Primary hematopoietic stem cells short term culture blood
22 chr9:95122400-95122600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
23 chr9:95122400-95129200 Weak transcription Primary T cells from cord blood blood
24 chr9:95122400-95131200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
25 chr9:95122400-95132200 Weak transcription Fetal Intestine Small intestine

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