Variant report

Variant rs9536196
Chromosome Location chr13:53183415-53183416
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:53175000-53191000 Weak transcription Fetal Stomach stomach
2 chr13:53181200-53190000 Weak transcription Monocytes-CD14+_RO01746 blood
3 chr13:53182200-53183800 Enhancers HUVEC blood vessel
4 chr13:53182400-53183600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
5 chr13:53182400-53186000 Enhancers Fetal Heart heart
6 chr13:53182800-53184400 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr13:53183000-53183600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
8 chr13:53183000-53183800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
9 chr13:53183200-53183600 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr13:53183200-53183600 Enhancers Brain Cingulate Gyrus brain
11 chr13:53183200-53183600 Enhancers Brain Inferior Temporal Lobe brain
12 chr13:53183200-53183600 Enhancers Rectal Mucosa Donor 31 rectum
13 chr13:53183200-53183600 Enhancers Skeletal Muscle Female skeletal muscle
14 chr13:53183200-53183600 Enhancers Stomach Smooth Muscle stomach
15 chr13:53183200-53183600 Flanking Active TSS HepG2 liver
16 chr13:53183200-53184400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
17 chr13:53183200-53184400 Enhancers Fetal Lung lung
18 chr13:53183400-53184000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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