Variant report

Variant rs16932620
Chromosome Location chr11:16171678-16171679
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16168800-16172600 Enhancers Fetal Lung lung
2 chr11:16169200-16174200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr11:16169800-16171800 Enhancers Fetal Intestine Small intestine
4 chr11:16169800-16174400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr11:16170000-16172000 Enhancers Fetal Muscle Leg muscle
6 chr11:16170400-16172600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
7 chr11:16170600-16171800 Enhancers Fetal Kidney kidney
8 chr11:16170600-16172400 Enhancers Cortex derived primary cultured neurospheres brain
9 chr11:16170800-16172200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
10 chr11:16170800-16175800 Weak transcription Muscle Satellite Cultured Cells --
11 chr11:16171000-16172000 Weak transcription Sigmoid Colon Sigmoid Colon
12 chr11:16171000-16173800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
13 chr11:16171000-16175200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr11:16171400-16172000 Enhancers Pancreatic Islets Pancreatic Islet
15 chr11:16171400-16172000 Enhancers Psoas Muscle Psoas
16 chr11:16171400-16173400 Weak transcription HepG2 liver
17 chr11:16171600-16175600 Weak transcription Fetal Intestine Large intestine

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