Variant report

Variant rs1957020
Chromosome Location chr14:32919375-32919376
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32908600-32920200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr14:32908600-32920200 Weak transcription Rectal Smooth Muscle rectum
3 chr14:32909000-32923400 Weak transcription Stomach Smooth Muscle stomach
4 chr14:32914400-32923000 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
5 chr14:32916400-32920200 Enhancers Colon Smooth Muscle Colon
6 chr14:32916400-32921000 Enhancers Brain Substantia Nigra brain
7 chr14:32916800-32919400 Enhancers Brain Inferior Temporal Lobe brain
8 chr14:32918800-32919400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr14:32918800-32919600 Enhancers Aorta Aorta
10 chr14:32918800-32920800 Enhancers Fetal Heart heart
11 chr14:32919000-32919400 Enhancers Left Ventricle heart
12 chr14:32919000-32919600 Enhancers Cortex derived primary cultured neurospheres brain
13 chr14:32919000-32919800 Enhancers Brain Cingulate Gyrus brain
14 chr14:32919000-32920800 Enhancers Brain Angular Gyrus brain
15 chr14:32919200-32919600 Weak transcription Fetal Lung lung
16 chr14:32919200-32919800 Weak transcription Brain Anterior Caudate brain
17 chr14:32919200-32920800 Enhancers Brain Hippocampus Middle brain
18 chr14:32919200-32926400 Weak transcription NHDF-Ad bronchial

Quick Search:


  
Input of quick search could be:

what's new

Quick links