Variant report

Variant rs1349138
Chromosome Location chr7:17544309-17544310
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17499400-17544600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr7:17537600-17546400 Weak transcription Ovary ovary
3 chr7:17538200-17544800 Weak transcription Stomach Mucosa stomach
4 chr7:17541000-17544600 Weak transcription Fetal Lung lung
5 chr7:17542200-17545800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr7:17542200-17547400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr7:17542800-17545800 Weak transcription NHLF lung
8 chr7:17542800-17547400 Enhancers Liver Liver
9 chr7:17543200-17548000 Enhancers HepG2 liver
10 chr7:17543600-17544600 Weak transcription Fetal Intestine Large intestine
11 chr7:17543600-17544600 Weak transcription Pancreatic Islets Pancreatic Islet
12 chr7:17543600-17545000 Weak transcription Fetal Intestine Small intestine
13 chr7:17543600-17550600 Weak transcription NHDF-Ad bronchial

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