Variant report

Variant rs13343966
Chromosome Location chr19:42996245-42996246
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:42981200-43002000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr19:42986000-42999400 Weak transcription Fetal Adrenal Gland Adrenal Gland
3 chr19:42986600-42998200 Weak transcription Liver Liver
4 chr19:42991000-43001000 Weak transcription Adipose Nuclei Adipose
5 chr19:42993000-43001400 Enhancers HepG2 liver
6 chr19:42993400-42997000 Weak transcription Fetal Intestine Small intestine
7 chr19:42993400-42997400 Weak transcription Fetal Intestine Large intestine
8 chr19:42993600-43000800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr19:42993800-42998600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
10 chr19:42993800-42999200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr19:42993800-43000800 Weak transcription A549 lung
12 chr19:42994000-42996400 Weak transcription Breast Myoepithelial Primary Cells Breast

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