Variant report

Variant rs17054972
Chromosome Location chr13:37703858-37703859
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:37700600-37704000 Enhancers Brain Angular Gyrus brain
2 chr13:37701000-37707200 Strong transcription Primary neutrophils fromperipheralblood blood
3 chr13:37701800-37709200 Weak transcription Fetal Kidney kidney
4 chr13:37702200-37704200 Enhancers Brain Inferior Temporal Lobe brain
5 chr13:37702200-37707600 Weak transcription Hela-S3 cervix
6 chr13:37702400-37708200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr13:37702600-37704000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr13:37702600-37704000 Enhancers Right Atrium heart
9 chr13:37702800-37704400 Enhancers HUVEC blood vessel
10 chr13:37702800-37707800 Weak transcription NH-A brain
11 chr13:37702800-37708000 Weak transcription Osteobl bone
12 chr13:37703400-37704000 Enhancers Brain Hippocampus Middle brain
13 chr13:37703400-37704000 Enhancers Brain Substantia Nigra brain
14 chr13:37703600-37704000 Enhancers Brain Anterior Caudate brain
15 chr13:37703600-37704200 Enhancers Brain Cingulate Gyrus brain
16 chr13:37703600-37708400 Weak transcription Fetal Lung lung
17 chr13:37703800-37704000 Enhancers Aorta Aorta
18 chr13:37703800-37704200 Enhancers Cortex derived primary cultured neurospheres brain
19 chr13:37703800-37704400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
20 chr13:37703800-37705400 Enhancers Colon Smooth Muscle Colon

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