Variant report

Variant rs17041539
Chromosome Location chr2:111552965-111552966
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:111531200-111566200 Weak transcription H9 Cell Line embryonic stem cell
2 chr2:111531600-111556800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr2:111531600-111558600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr2:111546800-111553000 Weak transcription Lung lung
5 chr2:111547200-111554000 Weak transcription Fetal Brain Female brain
6 chr2:111550600-111553000 Strong transcription iPS-18 Cell Line embryonic stem cell
7 chr2:111550800-111553000 Strong transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr2:111551200-111555000 Strong transcription HUES48 Cell Line embryonic stem cell
9 chr2:111551600-111553200 Strong transcription iPS-15b Cell Line embryonic stem cell
10 chr2:111551800-111553400 Enhancers Left Ventricle heart
11 chr2:111552200-111555400 Weak transcription HUES64 Cell Line embryonic stem cell
12 chr2:111552200-111556000 Weak transcription H1 Cell Line embryonic stem cell
13 chr2:111552400-111556200 Weak transcription iPS-20b Cell Line embryonic stem cell
14 chr2:111552400-111557800 Weak transcription Fetal Heart heart
15 chr2:111552600-111554000 Weak transcription Right Atrium heart
16 chr2:111552600-111567400 Weak transcription Right Ventricle heart
17 chr2:111552800-111554000 Weak transcription Fetal Brain Male brain
18 chr2:111552800-111554000 Weak transcription Pancreas Pancrea
19 chr2:111552800-111556200 Weak transcription HUES6 Cell Line embryonic stem cell

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