Variant report

Variant rs192985983
Chromosome Location chr12:31204402-31204403
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr12:31202800-31205000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr12:31203200-31207600 Enhancers Fetal Thymus thymus
6 chr12:31203800-31205600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
7 chr12:31204000-31205400 Weak transcription NH-A brain
8 chr12:31204200-31205000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr12:31204200-31206800 Enhancers Thymus Thymus
10 chr12:31204400-31205000 Enhancers H9 Cell Line embryonic stem cell
11 chr12:31204400-31205000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr12:31204400-31205000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr12:31204400-31205400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr12:31204400-31205400 Enhancers Primary B cells from peripheral blood blood
15 chr12:31204400-31205800 Enhancers Dnd41 blood

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