Variant report

Variant rs35955389
Chromosome Location chr2:173825951-173825952
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:173800600-173829400 Weak transcription Cortex derived primary cultured neurospheres brain
2 chr2:173807800-173831600 Weak transcription Left Ventricle heart
3 chr2:173816600-173831800 Weak transcription Lung lung
4 chr2:173819200-173827000 Weak transcription NHLF lung
5 chr2:173819600-173826800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:173819800-173826800 Weak transcription NHEK skin
7 chr2:173820800-173830400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
8 chr2:173822400-173835000 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr2:173823000-173832200 Weak transcription Brain Hippocampus Middle brain
10 chr2:173823200-173829600 Weak transcription Fetal Adrenal Gland Adrenal Gland
11 chr2:173824000-173830600 Weak transcription Brain Inferior Temporal Lobe brain
12 chr2:173824400-173827400 Weak transcription Adipose Nuclei Adipose
13 chr2:173825200-173830200 Weak transcription Brain Anterior Caudate brain
14 chr2:173825400-173826000 Enhancers Liver Liver
15 chr2:173825600-173829400 Enhancers HUVEC blood vessel

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