Variant report

Variant rs11893978
Chromosome Location chr2:50978621-50978622
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:50976200-50982800 Weak transcription Brain Substantia Nigra brain
2 chr2:50976600-50979800 Enhancers Fetal Stomach stomach
3 chr2:50976600-50983200 Weak transcription Brain Inferior Temporal Lobe brain
4 chr2:50977000-50982200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr2:50977400-50983600 Weak transcription Brain Hippocampus Middle brain
6 chr2:50977400-50984400 Enhancers Fetal Brain Female brain
7 chr2:50978200-50978800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr2:50978200-50979200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr2:50978200-50979200 Enhancers Colon Smooth Muscle Colon
10 chr2:50978200-50979400 Enhancers Duodenum Smooth Muscle Duodenum
11 chr2:50978200-50979600 Enhancers Rectal Smooth Muscle rectum
12 chr2:50978200-50980400 Enhancers Brain Germinal Matrix brain
13 chr2:50978200-50980400 Enhancers Pancreatic Islets Pancreatic Islet
14 chr2:50978400-50978800 Enhancers NH-A brain
15 chr2:50978400-50980800 Enhancers Cortex derived primary cultured neurospheres brain
16 chr2:50978400-50984400 Enhancers Fetal Brain Male brain
17 chr2:50978600-50978800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
18 chr2:50978600-50979200 Enhancers Fetal Muscle Leg muscle

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