Variant report

Variant rs576422156
Chromosome Location chr12:31205124-31205125
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31189800-31225400 Weak transcription Fetal Stomach stomach
2 chr12:31195000-31206200 Weak transcription Left Ventricle heart
3 chr12:31202200-31219400 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr12:31203200-31207600 Enhancers Fetal Thymus thymus
5 chr12:31203800-31205600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
6 chr12:31204000-31205400 Weak transcription NH-A brain
7 chr12:31204200-31206800 Enhancers Thymus Thymus
8 chr12:31204400-31205400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr12:31204400-31205400 Enhancers Primary B cells from peripheral blood blood
10 chr12:31204400-31205800 Enhancers Dnd41 blood
11 chr12:31204600-31205400 Enhancers Primary hematopoietic stem cells short term culture blood
12 chr12:31204600-31205400 Enhancers GM12878-XiMat blood
13 chr12:31204800-31205600 Enhancers iPS-15b Cell Line embryonic stem cell
14 chr12:31205000-31206000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr12:31205000-31206200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr12:31205000-31206200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
17 chr12:31205000-31206400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr12:31205000-31210400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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