Variant report

Variant rs28634753
Chromosome Location chr17:16587108-16587109
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:16581800-16589600 Weak transcription HUES48 Cell Line embryonic stem cell
2 chr17:16581800-16589800 Weak transcription HUES64 Cell Line embryonic stem cell
3 chr17:16586600-16587200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
4 chr17:16586600-16587200 Active TSS Ganglion Eminence derived primary cultured neurospheres brain
5 chr17:16586600-16587200 Active TSS Brain Hippocampus Middle brain
6 chr17:16586600-16587200 Active TSS Brain Inferior Temporal Lobe brain
7 chr17:16586600-16587200 Bivalent Enhancer Fetal Muscle Trunk muscle
8 chr17:16586600-16587400 Active TSS Brain Substantia Nigra brain
9 chr17:16586600-16587400 Bivalent/Poised TSS Fetal Brain Female brain
10 chr17:16586800-16587200 Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr17:16586800-16587200 Bivalent Enhancer Adipose Nuclei Adipose
12 chr17:16586800-16587200 Active TSS Brain Angular Gyrus brain
13 chr17:16586800-16587200 Bivalent Enhancer Left Ventricle heart
14 chr17:16586800-16587400 Enhancers Pancreas Pancrea
15 chr17:16586800-16587400 Bivalent Enhancer Sigmoid Colon Sigmoid Colon
16 chr17:16587000-16587200 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
17 chr17:16587000-16587200 Bivalent/Poised TSS Skeletal Muscle Male skeletal muscle
18 chr17:16587000-16587400 Bivalent Enhancer H1 Cell Line embryonic stem cell
19 chr17:16587000-16587400 Bivalent Enhancer Fetal Muscle Leg muscle
20 chr17:16587000-16587400 Enhancers HepG2 liver
21 chr17:16587000-16591400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links