Variant report

Variant rs12947654
Chromosome Location chr17:28568011-28568012
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:28563200-28575000 Weak transcription Aorta Aorta
2 chr17:28564800-28570600 Weak transcription Pancreas Pancrea
3 chr17:28564800-28573600 Weak transcription A549 lung
4 chr17:28565000-28570800 Weak transcription Right Atrium heart
5 chr17:28565600-28575000 Weak transcription Placenta Amnion Placenta Amnion
6 chr17:28565800-28572000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr17:28566000-28575400 Weak transcription H9 Cell Line embryonic stem cell
8 chr17:28566000-28575400 Weak transcription Gastric stomach
9 chr17:28566000-28575600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
10 chr17:28566200-28574000 Weak transcription GM12878-XiMat blood
11 chr17:28566200-28574200 Weak transcription Primary Natural Killer cells fromperipheralblood blood
12 chr17:28566200-28574800 Weak transcription Fetal Intestine Small intestine
13 chr17:28566400-28574400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
14 chr17:28566600-28618000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
15 chr17:28566800-28574400 Weak transcription HepG2 liver
16 chr17:28567000-28568200 Weak transcription Lung lung
17 chr17:28567000-28571600 Weak transcription Osteobl bone
18 chr17:28567200-28571800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
19 chr17:28567400-28570800 Weak transcription Placenta Placenta
20 chr17:28567600-28598000 Weak transcription ES-I3 Cell Line embryonic stem cell

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