Variant report

Variant rs10456546
Chromosome Location chr6:45217424-45217425
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:45208400-45218200 Weak transcription Gastric stomach
2 chr6:45211400-45220200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr6:45213800-45221200 Weak transcription Fetal Intestine Small intestine
4 chr6:45217000-45217600 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr6:45217200-45217600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr6:45217200-45217600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr6:45217200-45217600 Enhancers Psoas Muscle Psoas
8 chr6:45217200-45217600 Active TSS Osteobl bone
9 chr6:45217200-45218000 Enhancers HUES64 Cell Line embryonic stem cell
10 chr6:45217200-45218600 Enhancers HUES48 Cell Line embryonic stem cell
11 chr6:45217200-45218600 Enhancers Dnd41 blood
12 chr6:45217400-45217600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
13 chr6:45217400-45217800 Enhancers iPS-18 Cell Line embryonic stem cell

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