Variant report

Variant rs4076712
Chromosome Location chr9:140786918-140786919
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:140773200-140795400 Weak transcription Right Atrium heart
2 chr9:140777600-140787200 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
3 chr9:140778600-140787000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr9:140785400-140787000 Strong transcription iPS-15b Cell Line embryonic stem cell
5 chr9:140785600-140787400 Strong transcription Fetal Brain Female brain
6 chr9:140786000-140787000 Weak transcription Brain Inferior Temporal Lobe brain
7 chr9:140786600-140787000 Enhancers Brain Dorsolateral Prefrontal Cortex brain
8 chr9:140786600-140787600 Genic enhancers Brain Germinal Matrix brain
9 chr9:140786800-140787200 Enhancers Brain Cingulate Gyrus brain
10 chr9:140786800-140787400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
11 chr9:140786800-140787600 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell

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