Variant report

Variant rs2070443
Chromosome Location chr22:23776780-23776781
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:23774400-23777000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
2 chr22:23775000-23776800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr22:23775000-23777000 Enhancers Primary hematopoietic stem cells blood
4 chr22:23775000-23777000 Enhancers Primary hematopoietic stem cells short term culture blood
5 chr22:23775000-23778600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr22:23776200-23776800 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr22:23776200-23776800 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr22:23776200-23777000 Enhancers Fetal Thymus thymus
9 chr22:23776200-23777000 Enhancers Pancreas Pancrea
10 chr22:23776200-23779000 Weak transcription HUES6 Cell Line embryonic stem cell
11 chr22:23776200-23779800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr22:23776200-23780000 Weak transcription Primary monocytes fromperipheralblood blood
13 chr22:23776200-23780000 Weak transcription K562 blood
14 chr22:23776200-23780600 Weak transcription Fetal Stomach stomach
15 chr22:23776400-23776800 Enhancers Fetal Lung lung
16 chr22:23776400-23776800 Enhancers HepG2 liver
17 chr22:23776400-23777000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
18 chr22:23776400-23777000 Enhancers Dnd41 blood
19 chr22:23776600-23776800 Active TSS Rectal Mucosa Donor 29 rectum
20 chr22:23776600-23777000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin

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