Variant report

Variant rs1343355
Chromosome Location chr20:25725263-25725264
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:25700400-25725400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr20:25708000-25731400 Weak transcription Esophagus oesophagus
3 chr20:25713400-25731000 Weak transcription Left Ventricle heart
4 chr20:25714400-25731200 Weak transcription Pancreas Pancrea
5 chr20:25715600-25731400 Weak transcription Aorta Aorta
6 chr20:25720600-25725400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr20:25721000-25725400 Weak transcription NHEK skin
8 chr20:25721000-25725800 Weak transcription HMEC breast
9 chr20:25721000-25731000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr20:25724400-25726000 Enhancers Brain Cingulate Gyrus brain
11 chr20:25724400-25726000 Enhancers Brain Inferior Temporal Lobe brain
12 chr20:25724400-25727000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
13 chr20:25724400-25731400 Weak transcription Brain Angular Gyrus brain
14 chr20:25724600-25725600 Enhancers Brain Hippocampus Middle brain
15 chr20:25724600-25725600 Enhancers Brain Substantia Nigra brain
16 chr20:25724800-25725400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
17 chr20:25724800-25725600 Enhancers Brain Anterior Caudate brain

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