Variant report

Variant rs10409614
Chromosome Location chr19:20164165-20164166
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:20162600-20164200 Active TSS hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
2 chr19:20162600-20164200 Active TSS HUES64 Cell Line embryonic stem cell
3 chr19:20163600-20164200 Flanking Active TSS Fetal Intestine Small intestine
4 chr19:20164000-20164200 Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr19:20164000-20164200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr19:20164000-20164200 Enhancers Pancreas Pancrea
7 chr19:20164000-20166600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
8 chr19:20164000-20167800 Weak transcription Primary T regulatory cells fromperipheralblood blood
9 chr19:20164000-20170000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
10 chr19:20164000-20173400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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