Variant report

Variant rs62564441
Chromosome Location chr9:79056222-79056223
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:79049400-79056400 Weak transcription NH-A brain
2 chr9:79051400-79056600 Weak transcription HepG2 liver
3 chr9:79052600-79056600 Enhancers GM12878-XiMat blood
4 chr9:79053600-79057800 Weak transcription Fetal Intestine Small intestine
5 chr9:79055200-79056400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr9:79055400-79057000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr9:79055400-79057000 Enhancers Primary T helper 17 cells PMA-I stimulated --
8 chr9:79055400-79057400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr9:79055400-79057400 Enhancers Muscle Satellite Cultured Cells --
10 chr9:79055600-79056600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr9:79056000-79056600 Enhancers Osteobl bone

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