Variant report

Variant rs1790019
Chromosome Location chr6:162367823-162367824
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:162354200-162372200 Weak transcription Right Atrium heart
2 chr6:162364800-162377000 Weak transcription H9 Cell Line embryonic stem cell
3 chr6:162365400-162368600 Enhancers iPS-18 Cell Line embryonic stem cell
4 chr6:162366000-162370000 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr6:162366200-162368400 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr6:162366400-162368800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr6:162367200-162368200 Weak transcription HUES64 Cell Line embryonic stem cell
8 chr6:162367400-162368000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr6:162367400-162368000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
10 chr6:162367400-162368000 Enhancers Fetal Brain Male brain
11 chr6:162367600-162368600 Enhancers HUES48 Cell Line embryonic stem cell
12 chr6:162367800-162368400 Weak transcription H1 Cell Line embryonic stem cell
13 chr6:162367800-162368600 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr6:162367800-162368800 Enhancers iPS-15b Cell Line embryonic stem cell

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