Variant report

Variant rs73952884
Chromosome Location chr18:28791761-28791762
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:28787200-28805600 Weak transcription Pancreas Pancrea
2 chr18:28787600-28794600 Enhancers Fetal Intestine Large intestine
3 chr18:28787600-28797000 Weak transcription Right Atrium heart
4 chr18:28787800-28792600 Weak transcription HepG2 liver
5 chr18:28788000-28796600 Weak transcription Placenta Placenta
6 chr18:28788400-28792200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr18:28790400-28792400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
8 chr18:28790600-28791800 Enhancers Placenta Amnion Placenta Amnion
9 chr18:28790600-28794600 Enhancers Fetal Intestine Small intestine
10 chr18:28790800-28792000 Enhancers Fetal Heart heart
11 chr18:28790800-28792000 Enhancers Stomach Mucosa stomach
12 chr18:28791000-28791800 Enhancers HUES6 Cell Line embryonic stem cell
13 chr18:28791000-28791800 Enhancers Rectal Mucosa Donor 31 rectum
14 chr18:28791000-28791800 Enhancers NHEK skin
15 chr18:28791000-28793800 Enhancers Duodenum Mucosa Duodenum
16 chr18:28791200-28791800 Enhancers Right Ventricle heart
17 chr18:28791400-28796800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
18 chr18:28791400-28796800 Weak transcription Left Ventricle heart
19 chr18:28791400-28805600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
20 chr18:28791600-28793400 Weak transcription Small Intestine intestine

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