Variant report

Variant rs56337964
Chromosome Location chr6:45039786-45039787
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:45037000-45042400 Weak transcription Fetal Intestine Large intestine
2 chr6:45037800-45043000 Weak transcription Fetal Heart heart
3 chr6:45038800-45041000 Enhancers Primary T killer naive cells fromperipheralblood blood
4 chr6:45039200-45040000 Enhancers Fetal Adrenal Gland Adrenal Gland
5 chr6:45039200-45042600 Enhancers Dnd41 blood
6 chr6:45039200-45043000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr6:45039400-45040000 Enhancers Fetal Intestine Small intestine
8 chr6:45039400-45040200 Enhancers Primary monocytes fromperipheralblood blood
9 chr6:45039400-45040600 Enhancers Primary T helper cells fromperipheralblood blood
10 chr6:45039400-45040800 Enhancers Primary T helper memory cells from peripheral blood 2 blood
11 chr6:45039600-45039800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr6:45039600-45040200 Enhancers Monocytes-CD14+_RO01746 blood
13 chr6:45039600-45040400 Weak transcription Primary T helper naive cells fromperipheralblood blood
14 chr6:45039600-45040600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr6:45039600-45040800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr6:45039600-45041000 Enhancers Primary T helper cells PMA-I stimulated --
17 chr6:45039600-45042400 Weak transcription Primary T cells from cord blood blood

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