Variant report

Variant rs4604057
Chromosome Location chr4:20396598-20396599
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:20393200-20405800 Weak transcription Fetal Lung lung
2 chr4:20393200-20408800 Weak transcription Colon Smooth Muscle Colon
3 chr4:20395000-20398200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr4:20395200-20397000 Enhancers Brain Cingulate Gyrus brain
5 chr4:20395400-20396800 Enhancers iPS-18 Cell Line embryonic stem cell
6 chr4:20395600-20396600 Weak transcription Aorta Aorta
7 chr4:20395600-20396800 Weak transcription Brain Inferior Temporal Lobe brain
8 chr4:20395600-20399000 Weak transcription H1 Cell Line embryonic stem cell
9 chr4:20395600-20404800 Weak transcription NHDF-Ad bronchial
10 chr4:20395600-20405000 Weak transcription Brain Anterior Caudate brain
11 chr4:20395800-20396800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr4:20396200-20397000 Enhancers Brain Angular Gyrus brain
13 chr4:20396400-20396600 Enhancers Brain Substantia Nigra brain
14 chr4:20396400-20396800 Enhancers HUES48 Cell Line embryonic stem cell
15 chr4:20396400-20397000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
16 chr4:20396400-20397200 Enhancers Brain Hippocampus Middle brain

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