Variant report

Variant rs56058349
Chromosome Location chr11:17461663-17461664
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:17443800-17462600 Weak transcription Brain Substantia Nigra brain
2 chr11:17454000-17464000 Weak transcription Brain Anterior Caudate brain
3 chr11:17454200-17465800 Weak transcription Brain Angular Gyrus brain
4 chr11:17456000-17469200 Weak transcription Brain Inferior Temporal Lobe brain
5 chr11:17457000-17467200 Weak transcription Fetal Brain Male brain
6 chr11:17457200-17465400 Weak transcription Cortex derived primary cultured neurospheres brain
7 chr11:17457400-17464600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr11:17458800-17462000 Enhancers Fetal Thymus thymus
9 chr11:17460200-17462400 Strong transcription Fetal Brain Female brain
10 chr11:17460400-17462200 Enhancers A549 lung
11 chr11:17460800-17461800 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
12 chr11:17460800-17461800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr11:17460800-17462000 Weak transcription Pancreatic Islets Pancreatic Islet
14 chr11:17460800-17474000 Weak transcription Brain Cingulate Gyrus brain
15 chr11:17461200-17461800 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
16 chr11:17461200-17497400 Weak transcription Gastric stomach
17 chr11:17461400-17461800 Bivalent Enhancer Stomach Mucosa stomach
18 chr11:17461400-17462400 Weak transcription Dnd41 blood
19 chr11:17461600-17462000 Bivalent Enhancer Fetal Muscle Trunk muscle

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