Variant report

Variant rs73577431
Chromosome Location chr8:49750276-49750277
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49746200-49751000 Weak transcription Fetal Kidney kidney
2 chr8:49746800-49751000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr8:49746800-49751600 Weak transcription Pancreas Pancrea
4 chr8:49748000-49750600 Weak transcription Brain Germinal Matrix brain
5 chr8:49748000-49754600 Weak transcription Esophagus oesophagus
6 chr8:49748600-49751000 Weak transcription NH-A brain
7 chr8:49748600-49751200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr8:49748600-49751200 Weak transcription Fetal Muscle Leg muscle
9 chr8:49748800-49750600 Weak transcription Muscle Satellite Cultured Cells --
10 chr8:49748800-49750800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr8:49748800-49751000 Weak transcription HMEC breast
12 chr8:49748800-49751200 Weak transcription Fetal Lung lung
13 chr8:49748800-49751600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr8:49749000-49750800 Weak transcription NHEK skin
15 chr8:49749400-49751000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr8:49750200-49750400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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