Variant report

Variant rs9502331
Chromosome Location chr6:5717137-5717138
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:5707600-5724000 Weak transcription Thymus Thymus
2 chr6:5713400-5718200 Weak transcription Primary B cells from cord blood blood
3 chr6:5713800-5723400 Weak transcription Primary T cells from cord blood blood
4 chr6:5714000-5717200 Weak transcription Primary B cells from peripheral blood blood
5 chr6:5714600-5723600 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr6:5714800-5722800 Weak transcription H9 Cell Line embryonic stem cell
7 chr6:5715800-5718000 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr6:5716600-5717600 ZNF genes & repeats Primary hematopoietic stem cells short term culture blood
9 chr6:5716600-5717800 ZNF genes & repeats Fetal Intestine Small intestine
10 chr6:5716800-5717400 ZNF genes & repeats Fetal Stomach stomach
11 chr6:5716800-5717600 ZNF genes & repeats Breast Myoepithelial Primary Cells Breast
12 chr6:5717000-5717200 ZNF genes & repeats Fetal Muscle Leg muscle
13 chr6:5717000-5717400 ZNF genes & repeats H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
14 chr6:5717000-5717400 Enhancers Monocytes-CD14+_RO01746 blood
15 chr6:5717000-5717600 ZNF genes & repeats Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr6:5717000-5717600 ZNF genes & repeats Brain Substantia Nigra brain
17 chr6:5717000-5717600 ZNF genes & repeats Fetal Lung lung
18 chr6:5717000-5717800 Enhancers Primary monocytes fromperipheralblood blood

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