Variant report

Variant rs10143976
Chromosome Location chr14:37968636-37968637
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:37944400-37970800 Weak transcription Aorta Aorta
2 chr14:37959400-37970800 Weak transcription Stomach Smooth Muscle stomach
3 chr14:37959600-37970800 Weak transcription Pancreas Pancrea
4 chr14:37959800-37970800 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr14:37960200-37971000 Weak transcription Fetal Intestine Small intestine
6 chr14:37960200-37975400 Weak transcription HUVEC blood vessel
7 chr14:37963400-37970800 Weak transcription Ovary ovary
8 chr14:37963800-37969200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr14:37967200-37970200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr14:37967400-37969400 Weak transcription HepG2 liver
11 chr14:37967800-37970800 Weak transcription Skeletal Muscle Female skeletal muscle
12 chr14:37968200-37969600 Weak transcription Adipose Nuclei Adipose
13 chr14:37968200-37970800 Weak transcription Fetal Stomach stomach

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