Variant report

Variant rs56782665
Chromosome Location chr8:120439121-120439122
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:120431000-120439600 Weak transcription NHDF-Ad bronchial
2 chr8:120436000-120439600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
3 chr8:120436000-120439800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr8:120436800-120439400 Enhancers ES-I3 Cell Line embryonic stem cell
5 chr8:120437000-120439200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
6 chr8:120437000-120439600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr8:120437200-120440800 Weak transcription Pancreas Pancrea
8 chr8:120437400-120440000 Weak transcription Aorta Aorta
9 chr8:120437400-120440600 Weak transcription Fetal Adrenal Gland Adrenal Gland
10 chr8:120438000-120441000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
11 chr8:120438200-120439400 Enhancers HUES6 Cell Line embryonic stem cell
12 chr8:120438400-120439400 Enhancers Fetal Muscle Leg muscle
13 chr8:120438800-120440000 Weak transcription Fetal Lung lung
14 chr8:120438800-120440800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr8:120439000-120439200 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
16 chr8:120439000-120439200 Enhancers iPS-20b Cell Line embryonic stem cell

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