Variant report

Variant rs6887914
Chromosome Location chr5:112711486-112711487
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:112700800-112718000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr5:112707800-112719000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr5:112708000-112713800 Weak transcription HMEC breast
4 chr5:112708000-112714000 Weak transcription NHEK skin
5 chr5:112708000-112716200 Weak transcription Fetal Kidney kidney
6 chr5:112708600-112713400 Weak transcription HUVEC blood vessel
7 chr5:112710600-112714200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
8 chr5:112711000-112713200 Enhancers Dnd41 blood
9 chr5:112711200-112711600 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr5:112711200-112711600 Enhancers Fetal Stomach stomach
11 chr5:112711400-112711800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr5:112711400-112713000 Bivalent Enhancer Primary T cells from cord blood blood
13 chr5:112711400-112713400 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr5:112711400-112716200 Weak transcription NH-A brain

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