Variant report

Variant rs28432023
Chromosome Location chr7:17735224-17735225
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17730000-17737600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr7:17730400-17735600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr7:17730600-17735400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr7:17730600-17735400 Weak transcription Osteobl bone
5 chr7:17730600-17735600 Weak transcription NHDF-Ad bronchial
6 chr7:17730600-17735800 Weak transcription Hela-S3 cervix
7 chr7:17731800-17736200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr7:17735000-17735400 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr7:17735000-17735400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
10 chr7:17735000-17736200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
11 chr7:17735000-17737000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr7:17735000-17737200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr7:17735000-17737200 Enhancers HMEC breast
14 chr7:17735000-17737200 Enhancers NHEK skin
15 chr7:17735200-17737000 Enhancers Brain Substantia Nigra brain
16 chr7:17735200-17737200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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