Variant report

Variant rs11762032
Chromosome Location chr7:116669695-116669696
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:116661600-116670800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr7:116662000-116675200 Weak transcription Fetal Stomach stomach
3 chr7:116663600-116670600 Weak transcription Fetal Lung lung
4 chr7:116664000-116670800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
5 chr7:116665400-116670400 Weak transcription Brain Hippocampus Middle brain
6 chr7:116665800-116680600 Weak transcription Osteobl bone
7 chr7:116666200-116680400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr7:116666800-116673800 Weak transcription Pancreas Pancrea
9 chr7:116667000-116671200 Weak transcription Brain Inferior Temporal Lobe brain
10 chr7:116667000-116671200 Weak transcription Fetal Brain Male brain
11 chr7:116667000-116673800 Weak transcription Right Atrium heart
12 chr7:116667000-116674000 Weak transcription HUVEC blood vessel
13 chr7:116667000-116681000 Weak transcription NH-A brain
14 chr7:116667200-116669800 Weak transcription Fetal Heart heart
15 chr7:116667200-116671200 Weak transcription NHDF-Ad bronchial
16 chr7:116667200-116676000 Weak transcription K562 blood
17 chr7:116667200-116680800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
18 chr7:116669400-116674400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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