Variant report

Variant rs149863492
Chromosome Location chr12:31128162-31128163
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31108000-31130600 Weak transcription Fetal Brain Female brain
2 chr12:31117200-31128400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr12:31122800-31133600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr12:31124000-31129200 Weak transcription Brain Inferior Temporal Lobe brain
5 chr12:31124000-31129400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr12:31124000-31129400 Weak transcription HUES6 Cell Line embryonic stem cell
7 chr12:31124200-31128200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
8 chr12:31124200-31128800 Weak transcription Brain Cingulate Gyrus brain
9 chr12:31125000-31128600 Enhancers Fetal Heart heart
10 chr12:31126200-31128800 Weak transcription Brain Angular Gyrus brain
11 chr12:31126400-31130600 Weak transcription Spleen Spleen
12 chr12:31126800-31128600 Strong transcription Cortex derived primary cultured neurospheres brain
13 chr12:31127000-31128200 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived
14 chr12:31127000-31132600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr12:31127200-31128600 Weak transcription Fetal Stomach stomach
16 chr12:31127400-31128400 Strong transcription Brain Germinal Matrix brain
17 chr12:31127400-31130800 Weak transcription Colon Smooth Muscle Colon
18 chr12:31127600-31128200 Strong transcription Ganglion Eminence derived primary cultured neurospheres brain
19 chr12:31127600-31129400 Weak transcription ES-I3 Cell Line embryonic stem cell
20 chr12:31127600-31129600 Enhancers Right Ventricle heart
21 chr12:31128000-31128200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin

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