Variant report

Variant rs10863806
Chromosome Location chr1:210221413-210221414
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210213000-210221800 Weak transcription Brain Germinal Matrix brain
2 chr1:210213000-210223800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr1:210216800-210223000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr1:210217000-210221600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
5 chr1:210219200-210222400 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr1:210221000-210223600 Strong transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr1:210221200-210221800 ZNF genes & repeats ES-I3 Cell Line embryonic stem cell
8 chr1:210221200-210222000 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:210221400-210243200 Weak transcription iPS-18 Cell Line embryonic stem cell

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