Variant report

Variant rs11851991
Chromosome Location chr14:68566635-68566636
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:68547200-68567400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr14:68556400-68568400 Weak transcription Primary T cells from cord blood blood
3 chr14:68556600-68568000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr14:68561600-68568200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr14:68562200-68568400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr14:68564000-68567400 Enhancers Rectal Smooth Muscle rectum
7 chr14:68565400-68567000 Enhancers Cortex derived primary cultured neurospheres brain
8 chr14:68565600-68567000 Enhancers Fetal Kidney kidney
9 chr14:68565600-68567000 Enhancers Fetal Lung lung
10 chr14:68565600-68567200 Enhancers Fetal Muscle Leg muscle
11 chr14:68565600-68568600 Enhancers Colon Smooth Muscle Colon
12 chr14:68566000-68568000 ZNF genes & repeats ES-I3 Cell Line embryonic stem cell
13 chr14:68566400-68570000 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr14:68566600-68566800 Enhancers Stomach Smooth Muscle stomach
15 chr14:68566600-68570800 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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