Variant report

Variant rs41477950
Chromosome Location chr1:217105805-217105806
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:217088800-217112000 Weak transcription Pancreas Pancrea
2 chr1:217101200-217109600 Weak transcription HUES64 Cell Line embryonic stem cell
3 chr1:217102000-217107200 Weak transcription Fetal Intestine Small intestine
4 chr1:217103800-217109600 Weak transcription iPS-20b Cell Line embryonic stem cell
5 chr1:217104000-217109400 Weak transcription ES-I3 Cell Line embryonic stem cell
6 chr1:217104200-217109200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
7 chr1:217104200-217109600 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr1:217104600-217106200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:217105600-217106000 Enhancers NHEK skin
10 chr1:217105600-217106200 Enhancers HMEC breast

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