Variant report

Variant rs17626151
Chromosome Location chr1:76779444-76779445
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:76755800-76783000 Weak transcription Fetal Lung lung
2 chr1:76774200-76796400 Weak transcription Fetal Stomach stomach
3 chr1:76775400-76796400 Weak transcription Brain Substantia Nigra brain
4 chr1:76776400-76779600 Weak transcription Pancreatic Islets Pancreatic Islet
5 chr1:76778000-76782000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr1:76778400-76780200 Enhancers Fetal Heart heart
7 chr1:76778400-76783400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr1:76779000-76780600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr1:76779200-76779800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr1:76779200-76779800 Enhancers HUES48 Cell Line embryonic stem cell
11 chr1:76779200-76780200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
12 chr1:76779200-76780600 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
13 chr1:76779400-76779800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
14 chr1:76779400-76780000 Enhancers iPS-20b Cell Line embryonic stem cell
15 chr1:76779400-76780600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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