Variant report

Variant rs10489346
Chromosome Location chr1:210235308-210235309
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210221400-210243200 Weak transcription iPS-18 Cell Line embryonic stem cell
2 chr1:210223600-210245600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr1:210224400-210250000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:210234400-210235400 Weak transcription Pancreatic Islets Pancreatic Islet
5 chr1:210234400-210236000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
6 chr1:210234600-210235400 Weak transcription Brain Germinal Matrix brain
7 chr1:210235200-210235600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr1:210235200-210236000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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