Variant report

Variant rs538257910
Chromosome Location chr20:23643713-23643714
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:23637200-23660000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr20:23637800-23644200 Enhancers Fetal Intestine Large intestine
3 chr20:23638400-23644200 Enhancers Fetal Intestine Small intestine
4 chr20:23641800-23647000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr20:23641800-23647200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr20:23641800-23647200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr20:23641800-23652200 Weak transcription Adipose Nuclei Adipose
8 chr20:23642400-23644800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr20:23642400-23649400 Weak transcription Skeletal Muscle Male skeletal muscle
10 chr20:23642600-23647000 Weak transcription Primary monocytes fromperipheralblood blood
11 chr20:23642600-23647000 Weak transcription Monocytes-CD14+_RO01746 blood
12 chr20:23643000-23644000 Enhancers Fetal Muscle Trunk muscle
13 chr20:23643200-23644200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr20:23643200-23646000 Enhancers HepG2 liver
15 chr20:23643400-23646800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr20:23643600-23643800 Enhancers Fetal Muscle Leg muscle

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