Variant report

Variant rs2160996
Chromosome Location chr12:31105575-31105576
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31088200-31106600 Weak transcription Cortex derived primary cultured neurospheres brain
2 chr12:31098800-31106400 Weak transcription Brain Substantia Nigra brain
3 chr12:31099600-31116800 Weak transcription Fetal Stomach stomach
4 chr12:31100200-31111200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr12:31100800-31111200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr12:31103000-31106400 Weak transcription Right Atrium heart
7 chr12:31103800-31106000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
8 chr12:31103800-31106400 Weak transcription Fetal Brain Female brain
9 chr12:31104600-31105600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr12:31104600-31107800 Enhancers Duodenum Smooth Muscle Duodenum
11 chr12:31104600-31108200 Enhancers Thymus Thymus
12 chr12:31105000-31105800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr12:31105000-31105800 Weak transcription Brain Hippocampus Middle brain
14 chr12:31105000-31106000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr12:31105000-31106200 Weak transcription Rectal Smooth Muscle rectum
16 chr12:31105000-31106800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
17 chr12:31105000-31108200 Enhancers Fetal Thymus thymus
18 chr12:31105200-31105800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
19 chr12:31105200-31108200 Enhancers Fetal Heart heart

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