Variant report

Variant rs551438157
Chromosome Location chr8:130017002-130017003
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:130011800-130017200 Weak transcription Osteobl bone
2 chr8:130012000-130017200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr8:130012200-130017200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr8:130014600-130017200 Weak transcription Fetal Stomach stomach
5 chr8:130015400-130017200 Weak transcription Dnd41 blood
6 chr8:130016000-130017200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr8:130016000-130017200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr8:130016400-130017400 Weak transcription Fetal Muscle Leg muscle
9 chr8:130016600-130018400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
10 chr8:130017000-130018000 Enhancers HSMM muscle
11 chr8:130017000-130018200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr8:130017000-130018200 Enhancers Muscle Satellite Cultured Cells --
13 chr8:130017000-130018200 Enhancers Cortex derived primary cultured neurospheres brain
14 chr8:130017000-130018400 Enhancers HSMMtube muscle
15 chr8:130017000-130019600 Enhancers HMEC breast

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