Variant report

Variant rs1784598
Chromosome Location chr6:162374362-162374363
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:162364800-162377000 Weak transcription H9 Cell Line embryonic stem cell
2 chr6:162368000-162377200 Weak transcription Fetal Brain Male brain
3 chr6:162370200-162375000 Weak transcription Pancreas Pancrea
4 chr6:162371000-162384000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr6:162372400-162376000 Weak transcription Fetal Adrenal Gland Adrenal Gland
6 chr6:162372600-162375200 Weak transcription Right Atrium heart
7 chr6:162372600-162377000 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr6:162372600-162377000 Weak transcription HUES64 Cell Line embryonic stem cell
9 chr6:162372600-162377000 Weak transcription iPS-18 Cell Line embryonic stem cell
10 chr6:162372600-162377000 Weak transcription iPS-20b Cell Line embryonic stem cell
11 chr6:162372600-162377000 Weak transcription Cortex derived primary cultured neurospheres brain
12 chr6:162372600-162377200 Weak transcription iPS-15b Cell Line embryonic stem cell
13 chr6:162372800-162374600 Weak transcription HUES6 Cell Line embryonic stem cell

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