Variant report

Variant rs9913488
Chromosome Location chr17:34233451-34233452
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:34228200-34233600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr17:34229200-34236800 Weak transcription K562 blood
3 chr17:34229800-34240000 Weak transcription Primary T helper naive cells from peripheral blood blood
4 chr17:34230000-34245400 Weak transcription Primary T cells from cord blood blood
5 chr17:34230400-34233800 Weak transcription Fetal Thymus thymus
6 chr17:34231000-34233800 Weak transcription Primary T cells fromperipheralblood blood
7 chr17:34231400-34234000 Weak transcription Thymus Thymus
8 chr17:34231800-34234200 Enhancers Fetal Intestine Large intestine
9 chr17:34233000-34234000 Enhancers Fetal Intestine Small intestine
10 chr17:34233000-34234600 Enhancers Placenta Placenta
11 chr17:34233200-34235200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr17:34233400-34234600 Enhancers Primary Natural Killer cells fromperipheralblood blood
13 chr17:34233400-34234800 Enhancers Osteobl bone
14 chr17:34233400-34235200 Enhancers Placenta Amnion Placenta Amnion

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