Variant report

Variant rs546899381
Chromosome Location chr14:32951542-32951543
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32947600-32962200 Weak transcription Stomach Smooth Muscle stomach
2 chr14:32947800-32960600 Weak transcription Fetal Brain Male brain
3 chr14:32947800-32963400 Weak transcription Right Atrium heart
4 chr14:32950400-32951800 Enhancers Brain Hippocampus Middle brain
5 chr14:32950800-32951600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
6 chr14:32950800-32951600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr14:32950800-32951600 Enhancers Brain Anterior Caudate brain
8 chr14:32950800-32951600 Enhancers Brain Cingulate Gyrus brain
9 chr14:32950800-32960600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
10 chr14:32951000-32951600 Enhancers Brain Angular Gyrus brain
11 chr14:32951000-32951600 Enhancers Brain Inferior Temporal Lobe brain
12 chr14:32951000-32951600 Enhancers Brain Substantia Nigra brain
13 chr14:32951000-32951600 Enhancers Rectal Smooth Muscle rectum
14 chr14:32951000-32952000 Enhancers Cortex derived primary cultured neurospheres brain
15 chr14:32951200-32951800 Enhancers HUVEC blood vessel
16 chr14:32951400-32951600 Weak transcription Aorta Aorta
17 chr14:32951400-32951800 Enhancers Fetal Heart heart
18 chr14:32951400-32951800 Enhancers HSMMtube muscle
19 chr14:32951400-32952000 Enhancers Colon Smooth Muscle Colon
20 chr14:32951400-32960600 Weak transcription Left Ventricle heart

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