Variant report

Variant rs74182856
Chromosome Location chr2:113567532-113567533
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:113563400-113569200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr2:113563600-113569000 Weak transcription Esophagus oesophagus
3 chr2:113563600-113569200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr2:113565400-113568800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr2:113565600-113569000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:113565800-113568000 Enhancers HepG2 liver
7 chr2:113566400-113567600 Enhancers Primary monocytes fromperipheralblood blood
8 chr2:113566400-113572400 Enhancers Fetal Adrenal Gland Adrenal Gland
9 chr2:113566600-113569200 Weak transcription Small Intestine intestine
10 chr2:113567200-113568600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr2:113567200-113569400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr2:113567400-113568600 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr2:113567400-113568800 Weak transcription Fetal Lung lung
14 chr2:113567400-113568800 Weak transcription Monocytes-CD14+_RO01746 blood
15 chr2:113567400-113569000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr2:113567400-113569000 Weak transcription Pancreas Pancrea
17 chr2:113567400-113569000 Weak transcription Sigmoid Colon Sigmoid Colon
18 chr2:113567400-113569200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
19 chr2:113567400-113569200 Weak transcription Brain Cingulate Gyrus brain
20 chr2:113567400-113569400 Weak transcription Liver Liver
21 chr2:113567400-113570000 Weak transcription Brain Hippocampus Middle brain
22 chr2:113567400-113575800 Weak transcription Brain Substantia Nigra brain

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