Variant report

Variant rs150045884
Chromosome Location chr6:162376297-162376298
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr6:162371000-162384000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr6:162372600-162377000 Weak transcription HUES48 Cell Line embryonic stem cell
5 chr6:162372600-162377000 Weak transcription HUES64 Cell Line embryonic stem cell
6 chr6:162372600-162377000 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr6:162372600-162377000 Weak transcription iPS-20b Cell Line embryonic stem cell
8 chr6:162372600-162377000 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr6:162372600-162377200 Weak transcription iPS-15b Cell Line embryonic stem cell
10 chr6:162374600-162376400 Enhancers Left Ventricle heart
11 chr6:162374800-162380400 Weak transcription Gastric stomach
12 chr6:162375200-162377600 Enhancers Ovary ovary
13 chr6:162375200-162384800 Weak transcription Pancreas Pancrea
14 chr6:162375800-162376400 Enhancers Right Ventricle heart
15 chr6:162376000-162377600 Enhancers Fetal Adrenal Gland Adrenal Gland
16 chr6:162376200-162380200 Weak transcription Aorta Aorta
17 chr6:162376200-162384200 Weak transcription Right Atrium heart

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