Variant report

Variant rs17012409
Chromosome Location chr2:33189370-33189371
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:33173800-33192000 Weak transcription Liver Liver
2 chr2:33174400-33191000 Weak transcription HUVEC blood vessel
3 chr2:33174400-33196600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
4 chr2:33184400-33191400 Weak transcription Stomach Smooth Muscle stomach
5 chr2:33185600-33189400 Enhancers Fetal Heart heart
6 chr2:33188200-33189800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr2:33188200-33190400 Weak transcription Brain Hippocampus Middle brain
8 chr2:33188200-33191200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr2:33188400-33190000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
10 chr2:33188800-33189400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr2:33188800-33189400 Enhancers Colon Smooth Muscle Colon
12 chr2:33188800-33189600 Enhancers NHLF lung
13 chr2:33188800-33189600 Enhancers Osteobl bone
14 chr2:33188800-33190000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr2:33189000-33189600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr2:33189000-33189600 Enhancers Muscle Satellite Cultured Cells --

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