Variant report

Variant rs28676827
Chromosome Location chr7:16994780-16994781
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:16988600-17009000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr7:16991200-17002200 Weak transcription Stomach Mucosa stomach
3 chr7:16992000-16995800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr7:16992000-16999800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr7:16992000-16999800 Weak transcription Osteobl bone
6 chr7:16993000-16995600 Enhancers Fetal Heart heart
7 chr7:16993400-16995000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
8 chr7:16993400-16995000 Enhancers Fetal Muscle Leg muscle
9 chr7:16993600-16994800 Enhancers Stomach Smooth Muscle stomach
10 chr7:16993800-16994800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr7:16993800-16994800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr7:16993800-16995000 Weak transcription Left Ventricle heart
13 chr7:16994000-16994800 Enhancers Skeletal Muscle Male skeletal muscle
14 chr7:16994000-16998000 Weak transcription HepG2 liver
15 chr7:16994200-16995400 Weak transcription NHDF-Ad bronchial
16 chr7:16994400-16999200 Weak transcription HSMMtube muscle
17 chr7:16994400-17000000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
18 chr7:16994600-16994800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
19 chr7:16994600-16994800 Enhancers Fetal Stomach stomach

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