Variant report

Variant rs371495378
Chromosome Location chr6:162375432-162375433
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr6:162372400-162376000 Weak transcription Fetal Adrenal Gland Adrenal Gland
5 chr6:162372600-162377000 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr6:162372600-162377000 Weak transcription HUES64 Cell Line embryonic stem cell
7 chr6:162372600-162377000 Weak transcription iPS-18 Cell Line embryonic stem cell
8 chr6:162372600-162377000 Weak transcription iPS-20b Cell Line embryonic stem cell
9 chr6:162372600-162377000 Weak transcription Cortex derived primary cultured neurospheres brain
10 chr6:162372600-162377200 Weak transcription iPS-15b Cell Line embryonic stem cell
11 chr6:162374600-162376400 Enhancers Left Ventricle heart
12 chr6:162374800-162380400 Weak transcription Gastric stomach
13 chr6:162375200-162375600 Enhancers Fetal Brain Female brain
14 chr6:162375200-162376200 Enhancers Right Atrium heart
15 chr6:162375200-162377600 Enhancers Ovary ovary
16 chr6:162375200-162384800 Weak transcription Pancreas Pancrea

Quick Search:


  
Input of quick search could be:

what's new

Quick links