Variant report

Variant rs6493512
Chromosome Location chr15:51904611-51904612
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr15:51894000-51906000 Weak transcription Dnd41 blood
5 chr15:51895000-51911600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr15:51895200-51913000 Weak transcription HMEC breast
7 chr15:51897200-51910800 Weak transcription A549 lung
8 chr15:51902600-51909600 Weak transcription K562 blood
9 chr15:51903600-51913600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr15:51903800-51905200 ZNF genes & repeats Primary hematopoietic stem cells blood
11 chr15:51904000-51905200 ZNF genes & repeats Primary monocytes fromperipheralblood blood
12 chr15:51904000-51905200 ZNF genes & repeats Fetal Intestine Small intestine
13 chr15:51904200-51907400 Weak transcription Pancreatic Islets Pancreatic Islet
14 chr15:51904200-51911600 Weak transcription Brain Germinal Matrix brain
15 chr15:51904200-51914000 Weak transcription Lung lung
16 chr15:51904400-51904800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
17 chr15:51904400-51912800 Weak transcription Fetal Stomach stomach
18 chr15:51904600-51904800 Weak transcription Monocytes-CD14+_RO01746 blood

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