Variant report

Variant rs62445141
Chromosome Location chr7:17060050-17060051
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr7:17055400-17060800 Weak transcription Primary T helper 17 cells PMA-I stimulated --
3 chr7:17056600-17060400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr7:17056800-17061000 Weak transcription Osteobl bone
5 chr7:17058800-17062800 Enhancers HepG2 liver
6 chr7:17059000-17060200 Enhancers NHDF-Ad bronchial
7 chr7:17059000-17060400 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr7:17059000-17060600 Enhancers HUVEC blood vessel
9 chr7:17059600-17063000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr7:17059800-17060600 Enhancers Fetal Intestine Small intestine
11 chr7:17059800-17062000 Enhancers Liver Liver
12 chr7:17059800-17062800 Enhancers HMEC breast
13 chr7:17060000-17060600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr7:17060000-17060600 Enhancers Fetal Intestine Large intestine
15 chr7:17060000-17060600 Enhancers Stomach Mucosa stomach
16 chr7:17060000-17061600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
17 chr7:17060000-17061600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr7:17060000-17061600 Enhancers NHEK skin

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