Variant report

Variant rs56407806
Chromosome Location chr2:173729102-173729103
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:173726000-173734400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr2:173726200-173734400 Weak transcription NHEK skin
3 chr2:173726200-173734600 Weak transcription HUVEC blood vessel
4 chr2:173726800-173753600 Weak transcription Brain Angular Gyrus brain
5 chr2:173727800-173729600 Weak transcription Lung lung
6 chr2:173727800-173733400 Weak transcription Fetal Adrenal Gland Adrenal Gland
7 chr2:173728000-173729200 Enhancers Fetal Intestine Small intestine
8 chr2:173728000-173729600 Enhancers Fetal Intestine Large intestine
9 chr2:173728800-173729200 Enhancers Small Intestine intestine
10 chr2:173729000-173729200 Enhancers Pancreas Pancrea
11 chr2:173729000-173729600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
12 chr2:173729000-173729600 Enhancers Left Ventricle heart
13 chr2:173729000-173730000 Enhancers Duodenum Mucosa Duodenum
14 chr2:173729000-173730000 Enhancers Gastric stomach
15 chr2:173729000-173735000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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