Variant report

Variant rs62369676
Chromosome Location chr5:16511309-16511310
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:16508800-16511600 Enhancers Primary T helper cells PMA-I stimulated --
2 chr5:16509200-16524200 Weak transcription Brain Cingulate Gyrus brain
3 chr5:16509400-16513000 Weak transcription Right Ventricle heart
4 chr5:16509400-16515600 Weak transcription Brain Inferior Temporal Lobe brain
5 chr5:16509600-16515600 Weak transcription Brain Substantia Nigra brain
6 chr5:16509600-16528800 Weak transcription Brain Hippocampus Middle brain
7 chr5:16509800-16513600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr5:16509800-16521000 Weak transcription Fetal Heart heart
9 chr5:16510000-16512000 Weak transcription Left Ventricle heart
10 chr5:16510200-16511600 Weak transcription Fetal Intestine Small intestine
11 chr5:16511000-16511600 Genic enhancers Primary T cells from cord blood blood
12 chr5:16511000-16512400 Enhancers Primary T helper naive cells fromperipheralblood blood
13 chr5:16511200-16519200 Weak transcription Fetal Intestine Large intestine

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