Variant report

Variant rs11238756
Chromosome Location chr10:44367287-44367288
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:44360000-44392200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr10:44361800-44373000 Weak transcription Fetal Heart heart
3 chr10:44364200-44374000 Weak transcription NHLF lung
4 chr10:44365000-44373400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr10:44365000-44373400 Weak transcription Right Ventricle heart
6 chr10:44365400-44371400 Weak transcription NHDF-Ad bronchial
7 chr10:44365800-44367400 Enhancers Fetal Stomach stomach
8 chr10:44365800-44368400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr10:44366000-44368400 Enhancers Brain Inferior Temporal Lobe brain
10 chr10:44366400-44368600 Enhancers Brain Hippocampus Middle brain
11 chr10:44366600-44367400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
12 chr10:44366600-44367400 Enhancers Brain Germinal Matrix brain
13 chr10:44366800-44367600 Enhancers Fetal Muscle Trunk muscle
14 chr10:44366800-44371400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr10:44367200-44368200 Weak transcription Brain Cingulate Gyrus brain
16 chr10:44367200-44373200 Weak transcription Left Ventricle heart
17 chr10:44367200-44373200 Weak transcription Right Atrium heart
18 chr10:44367200-44373200 Weak transcription Spleen Spleen

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