Variant report

Variant rs569787
Chromosome Location chr8:102875821-102875822
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:102862800-102876000 Weak transcription H1 Cell Line embryonic stem cell
2 chr8:102866600-102876000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr8:102869200-102880200 Weak transcription Aorta Aorta
4 chr8:102870000-102891200 Weak transcription Ovary ovary
5 chr8:102870600-102879000 Weak transcription Small Intestine intestine
6 chr8:102871000-102880400 Weak transcription Psoas Muscle Psoas
7 chr8:102871000-102880800 Weak transcription Primary Natural Killer cells fromperipheralblood blood
8 chr8:102871200-102876000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr8:102874600-102876800 Enhancers HSMMtube muscle
10 chr8:102874800-102876600 Enhancers NHDF-Ad bronchial
11 chr8:102875000-102876800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr8:102875200-102876600 Enhancers Fetal Muscle Leg muscle
13 chr8:102875800-102876400 Enhancers iPS-18 Cell Line embryonic stem cell
14 chr8:102875800-102876400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr8:102875800-102876600 Enhancers ES-I3 Cell Line embryonic stem cell

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