Variant report

Variant rs9526898
Chromosome Location chr13:52934912-52934913
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:52931000-52935400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr13:52931200-52935200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr13:52931400-52935200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr13:52931400-52935200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr13:52931400-52935400 Weak transcription HMEC breast
6 chr13:52931400-52935400 Weak transcription NHEK skin
7 chr13:52931400-52935600 Weak transcription Osteobl bone
8 chr13:52931400-52937200 Weak transcription NH-A brain
9 chr13:52934000-52951800 Weak transcription Fetal Intestine Small intestine
10 chr13:52934400-52940400 Weak transcription Fetal Lung lung
11 chr13:52934600-52944800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr13:52934800-52940400 Weak transcription Fetal Muscle Leg muscle

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