Variant report

Variant rs17099754
Chromosome Location chr1:77412349-77412350
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:77393400-77429000 Weak transcription Aorta Aorta
2 chr1:77405400-77427000 Weak transcription Fetal Stomach stomach
3 chr1:77408600-77414600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr1:77410200-77412400 Enhancers Cortex derived primary cultured neurospheres brain
5 chr1:77410200-77421200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr1:77410400-77412600 Enhancers Pancreatic Islets Pancreatic Islet
7 chr1:77410800-77415000 Weak transcription NHLF lung
8 chr1:77411000-77414600 Weak transcription Muscle Satellite Cultured Cells --
9 chr1:77411000-77414600 Weak transcription HSMM muscle
10 chr1:77411000-77415000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr1:77411000-77416600 Weak transcription Ovary ovary
12 chr1:77411200-77413800 Weak transcription NHDF-Ad bronchial
13 chr1:77411200-77414000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr1:77411200-77414600 Weak transcription Osteobl bone
15 chr1:77411600-77414600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr1:77411800-77421000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
17 chr1:77412200-77421400 Weak transcription HUES48 Cell Line embryonic stem cell
18 chr1:77412200-77427000 Weak transcription ES-I3 Cell Line embryonic stem cell

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