Variant report

Variant rs1721014
Chromosome Location chr7:17008921-17008922
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr7:17001400-17025600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr7:17003000-17015200 Weak transcription Small Intestine intestine
4 chr7:17005600-17010400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr7:17005600-17011600 Enhancers NHDF-Ad bronchial
6 chr7:17005800-17010400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr7:17006000-17018600 Weak transcription Esophagus oesophagus
8 chr7:17006600-17010400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr7:17008000-17018600 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr7:17008200-17010400 Weak transcription Osteobl bone
11 chr7:17008200-17010800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr7:17008200-17011400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr7:17008200-17018800 Weak transcription Aorta Aorta
14 chr7:17008600-17010400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
15 chr7:17008600-17018800 Weak transcription Right Atrium heart
16 chr7:17008800-17010400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr7:17008800-17018200 Weak transcription HSMMtube muscle

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