Variant report

Variant rs59002304
Chromosome Location chr8:125791379-125791380
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:125774200-125795800 Weak transcription Pancreas Pancrea
2 chr8:125785000-125793000 Weak transcription Esophagus oesophagus
3 chr8:125785000-125793200 Weak transcription Rectal Mucosa Donor 31 rectum
4 chr8:125785000-125794000 Weak transcription Primary B cells from cord blood blood
5 chr8:125785000-125794600 Weak transcription Pancreatic Islets Pancreatic Islet
6 chr8:125787400-125792200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr8:125788200-125792000 Weak transcription HepG2 liver
8 chr8:125788400-125793200 Weak transcription Fetal Intestine Small intestine
9 chr8:125788600-125791800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr8:125788600-125793400 Weak transcription Fetal Intestine Large intestine
11 chr8:125788800-125793200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr8:125788800-125795000 Weak transcription Spleen Spleen
13 chr8:125788800-125796800 Weak transcription Brain Cingulate Gyrus brain
14 chr8:125788800-125797000 Weak transcription Left Ventricle heart
15 chr8:125791200-125795800 Enhancers Placenta Placenta

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