Variant report

Variant rs56102090
Chromosome Location chr8:49048963-49048964
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49043600-49049000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr8:49043800-49049600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr8:49044600-49051600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr8:49048400-49050000 Enhancers Gastric stomach
5 chr8:49048400-49050200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr8:49048400-49050200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr8:49048600-49049200 Enhancers Primary T cells from cord blood blood
8 chr8:49048800-49049000 Bivalent Enhancer Primary T cells fromperipheralblood blood
9 chr8:49048800-49049200 Flanking Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr8:49048800-49049400 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr8:49048800-49049400 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr8:49048800-49049800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr8:49048800-49049800 Enhancers HepG2 liver
14 chr8:49048800-49050000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr8:49048800-49050400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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