Variant report

Variant rs28891769
Chromosome Location chr15:44072860-44072861
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:44068800-44073200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr15:44070200-44083800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr15:44070200-44083800 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr15:44070200-44083800 Weak transcription Rectal Smooth Muscle rectum
5 chr15:44070200-44083800 Weak transcription NHDF-Ad bronchial
6 chr15:44070200-44083800 Weak transcription NHEK skin
7 chr15:44070600-44083600 Weak transcription Primary hematopoietic stem cells short term culture blood
8 chr15:44070600-44083800 Weak transcription Rectal Mucosa Donor 29 rectum
9 chr15:44070800-44074800 Weak transcription Primary B cells from peripheral blood blood
10 chr15:44070800-44083600 Weak transcription Primary T cells fromperipheralblood blood
11 chr15:44071600-44079000 Weak transcription GM12878-XiMat blood
12 chr15:44071600-44083600 Weak transcription Dnd41 blood
13 chr15:44071600-44083600 Weak transcription Hela-S3 cervix
14 chr15:44071600-44083800 Weak transcription Primary T helper cells fromperipheralblood blood
15 chr15:44072800-44073000 Enhancers Fetal Intestine Large intestine
16 chr15:44072800-44073600 Enhancers K562 blood

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