Variant report

Variant rs1790008
Chromosome Location chr6:162377377-162377378
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:162371000-162384000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:162374800-162380400 Weak transcription Gastric stomach
3 chr6:162375200-162377600 Enhancers Ovary ovary
4 chr6:162375200-162384800 Weak transcription Pancreas Pancrea
5 chr6:162376000-162377600 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr6:162376200-162380200 Weak transcription Aorta Aorta
7 chr6:162376200-162384200 Weak transcription Right Atrium heart
8 chr6:162376400-162379400 Weak transcription Left Ventricle heart
9 chr6:162377000-162377400 Enhancers H9 Cell Line embryonic stem cell
10 chr6:162377000-162377400 Enhancers HUES48 Cell Line embryonic stem cell
11 chr6:162377000-162377400 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr6:162377000-162377600 Enhancers HUES6 Cell Line embryonic stem cell
13 chr6:162377000-162377600 Enhancers HUES64 Cell Line embryonic stem cell
14 chr6:162377000-162377600 Enhancers iPS-18 Cell Line embryonic stem cell
15 chr6:162377000-162377600 Enhancers Cortex derived primary cultured neurospheres brain
16 chr6:162377200-162377400 Enhancers Fetal Brain Male brain
17 chr6:162377200-162377600 Enhancers iPS-15b Cell Line embryonic stem cell
18 chr6:162377200-162384000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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