Variant report

Variant rs56676438
Chromosome Location chr2:210425286-210425287
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210410600-210430800 Weak transcription Fetal Brain Female brain
2 chr2:210415000-210429800 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr2:210419400-210430800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr2:210421400-210430800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
5 chr2:210422600-210425800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr2:210424400-210425800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
7 chr2:210424600-210426400 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr2:210424800-210425400 Enhancers Brain Germinal Matrix brain
9 chr2:210425000-210427800 Weak transcription Cortex derived primary cultured neurospheres brain
10 chr2:210425200-210426400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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