Variant report

Variant rs1509465
Chromosome Location chr2:210476185-210476186
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr2:210465800-210477200 Weak transcription HUES48 Cell Line embryonic stem cell
3 chr2:210465800-210477800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr2:210466400-210476400 Weak transcription iPS-18 Cell Line embryonic stem cell
5 chr2:210467800-210476400 Weak transcription Fetal Brain Female brain
6 chr2:210469800-210478600 Weak transcription Brain Germinal Matrix brain
7 chr2:210474000-210481400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr2:210474200-210476800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr2:210474400-210476600 Genic enhancers Cortex derived primary cultured neurospheres brain
10 chr2:210474800-210476800 Genic enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr2:210475000-210477600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
12 chr2:210475200-210477400 Weak transcription iPS-15b Cell Line embryonic stem cell
13 chr2:210475200-210478600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
14 chr2:210475400-210478200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
15 chr2:210475600-210478800 Enhancers HUES64 Cell Line embryonic stem cell

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