Variant report

Variant rs17137084
Chromosome Location chr7:17061526-17061527
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17050600-17071800 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
2 chr7:17058800-17062800 Enhancers HepG2 liver
3 chr7:17059600-17063000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:17059800-17062000 Enhancers Liver Liver
5 chr7:17059800-17062800 Enhancers HMEC breast
6 chr7:17060000-17061600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr7:17060000-17061600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr7:17060000-17061600 Enhancers NHEK skin
9 chr7:17060800-17063800 Enhancers Primary T helper 17 cells PMA-I stimulated --
10 chr7:17061200-17061600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr7:17061400-17061600 Enhancers Fetal Intestine Small intestine
12 chr7:17061400-17061600 Enhancers Stomach Mucosa stomach
13 chr7:17061400-17064200 Enhancers Breast Myoepithelial Primary Cells Breast

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