Variant report

Variant rs7603837
Chromosome Location chr2:210467214-210467215
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210460600-210477400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr2:210461800-210469400 Weak transcription Brain Angular Gyrus brain
3 chr2:210465000-210467600 Genic enhancers H9 Derived Neuron Cultured Cells ES cell derived
4 chr2:210465000-210467800 Enhancers Fetal Brain Male brain
5 chr2:210465400-210468400 Weak transcription iPS-20b Cell Line embryonic stem cell
6 chr2:210465400-210475200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr2:210465600-210467800 Enhancers Brain Germinal Matrix brain
8 chr2:210465800-210475000 Weak transcription HUES64 Cell Line embryonic stem cell
9 chr2:210465800-210477200 Weak transcription HUES48 Cell Line embryonic stem cell
10 chr2:210465800-210477800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr2:210466000-210467800 Enhancers Fetal Brain Female brain
12 chr2:210466400-210476400 Weak transcription iPS-18 Cell Line embryonic stem cell
13 chr2:210466600-210469200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr2:210467000-210467600 Strong transcription Cortex derived primary cultured neurospheres brain
15 chr2:210467000-210468400 Strong transcription Ganglion Eminence derived primary cultured neurospheres brain
16 chr2:210467000-210469200 ZNF genes & repeats H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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