Variant report

Variant rs144821836
Chromosome Location chr8:3141616-3141617
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:3141400-3142200 Active TSS Brain Inferior Temporal Lobe brain
2 chr8:3141600-3141800 Enhancers HUES6 Cell Line embryonic stem cell
3 chr8:3141600-3141800 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
4 chr8:3141600-3141800 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
5 chr8:3141600-3141800 Active TSS Brain Cingulate Gyrus brain
6 chr8:3141600-3141800 Enhancers Brain Hippocampus Middle brain
7 chr8:3141600-3141800 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr8:3141600-3141800 Enhancers Fetal Brain Male brain
9 chr8:3141600-3141800 Active TSS Fetal Brain Female brain
10 chr8:3141600-3141800 Active TSS Fetal Lung lung
11 chr8:3141600-3142000 Enhancers H1 Cell Line embryonic stem cell
12 chr8:3141600-3142000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr8:3141600-3142000 Active TSS Brain Germinal Matrix brain
14 chr8:3141600-3142000 Active TSS Duodenum Mucosa Duodenum
15 chr8:3141600-3142000 Flanking Active TSS Fetal Muscle Trunk muscle
16 chr8:3141600-3142200 Active TSS Breast Myoepithelial Primary Cells Breast
17 chr8:3141600-3142200 Active TSS Brain Dorsolateral Prefrontal Cortex brain
18 chr8:3141600-3142200 Flanking Active TSS Fetal Kidney kidney

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