Variant report

Variant rs4099522
Chromosome Location chr18:404777-404778
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:393200-433000 Weak transcription Fetal Brain Male brain
2 chr18:396000-406800 Weak transcription Brain Substantia Nigra brain
3 chr18:396000-406800 Weak transcription Right Atrium heart
4 chr18:397600-406000 Enhancers Primary neutrophils fromperipheralblood blood
5 chr18:399200-409800 Weak transcription Duodenum Smooth Muscle Duodenum
6 chr18:400200-405200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr18:400400-404800 Strong transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr18:401000-404800 Strong transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr18:402000-406800 Weak transcription NHDF-Ad bronchial
10 chr18:403000-405000 Weak transcription Fetal Muscle Trunk muscle
11 chr18:403000-405400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr18:403200-405400 Weak transcription Fetal Stomach stomach
13 chr18:403400-405000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr18:403600-405200 Weak transcription Fetal Lung lung
15 chr18:403800-405000 Enhancers Primary monocytes fromperipheralblood blood
16 chr18:403800-405800 Enhancers Monocytes-CD14+_RO01746 blood
17 chr18:403800-407200 Enhancers Placenta Placenta
18 chr18:404400-406000 ZNF genes & repeats Fetal Muscle Leg muscle

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