Variant report

Variant rs2465922
Chromosome Location chr7:137871149-137871150
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:137867000-137871400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
2 chr7:137867200-137871400 Weak transcription iPS-18 Cell Line embryonic stem cell
3 chr7:137867200-137871400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr7:137867400-137871200 Weak transcription iPS-20b Cell Line embryonic stem cell
5 chr7:137867400-137871400 Weak transcription HUES64 Cell Line embryonic stem cell
6 chr7:137869400-137871600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
7 chr7:137869800-137873000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr7:137870000-137871200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr7:137870000-137872400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr7:137870200-137872400 Enhancers NH-A brain
11 chr7:137870400-137872800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr7:137870800-137871200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
13 chr7:137870800-137871800 Enhancers Placenta Amnion Placenta Amnion
14 chr7:137871000-137872200 Enhancers Cortex derived primary cultured neurospheres brain

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