Variant report

Variant rs1721028
Chromosome Location chr7:16993426-16993427
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 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 chr7:16991800-16993800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr7:16991800-16993800 Weak transcription Duodenum Smooth Muscle Duodenum
5 chr7:16991800-16994200 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr7:16992000-16993800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr7:16992000-16993800 Weak transcription NHDF-Ad bronchial
8 chr7:16992000-16994600 Weak transcription Fetal Stomach stomach
9 chr7:16992000-16995800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr7:16992000-16999800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr7:16992000-16999800 Weak transcription Osteobl bone
12 chr7:16992600-16993800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
13 chr7:16992600-16994600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
14 chr7:16993000-16994000 Enhancers HepG2 liver
15 chr7:16993000-16995600 Enhancers Fetal Heart heart
16 chr7:16993200-16993800 Enhancers Left Ventricle heart
17 chr7:16993200-16993800 Enhancers Right Atrium heart
18 chr7:16993400-16994400 Enhancers HSMMtube muscle
19 chr7:16993400-16995000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
20 chr7:16993400-16995000 Enhancers Fetal Muscle Leg muscle

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