Variant report

Variant rs2899476
Chromosome Location chr15:51903874-51903875
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:51889400-51909400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr15:51892600-51913000 Weak transcription Rectal Mucosa Donor 31 rectum
3 chr15:51893000-51911000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr15:51893800-51904000 Weak transcription Fetal Stomach stomach
5 chr15:51894000-51906000 Weak transcription Dnd41 blood
6 chr15:51895000-51911600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr15:51895200-51913000 Weak transcription HMEC breast
8 chr15:51896000-51904000 Weak transcription Lung lung
9 chr15:51897200-51910800 Weak transcription A549 lung
10 chr15:51902200-51904000 Weak transcription Primary monocytes fromperipheralblood blood
11 chr15:51902400-51904000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
12 chr15:51902600-51909600 Weak transcription K562 blood
13 chr15:51903600-51904200 Strong transcription Monocytes-CD14+_RO01746 blood
14 chr15:51903600-51913600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
15 chr15:51903800-51905200 ZNF genes & repeats Primary hematopoietic stem cells blood

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