Variant report

Variant rs16932630
Chromosome Location chr11:16173986-16173987
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16169200-16174200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr11:16169800-16174400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr11:16170800-16175800 Weak transcription Muscle Satellite Cultured Cells --
4 chr11:16171000-16175200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr11:16171600-16175600 Weak transcription Fetal Intestine Large intestine
6 chr11:16172400-16176000 Weak transcription Fetal Intestine Small intestine
7 chr11:16172400-16191400 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr11:16172600-16191400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
9 chr11:16173000-16174400 Enhancers A549 lung
10 chr11:16173400-16175600 Enhancers HepG2 liver
11 chr11:16173800-16174000 Enhancers Ovary ovary
12 chr11:16173800-16174000 Enhancers Psoas Muscle Psoas
13 chr11:16173800-16174000 Enhancers HMEC breast
14 chr11:16173800-16174600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
15 chr11:16173800-16175400 Weak transcription Pancreatic Islets Pancreatic Islet

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