Variant report

Variant rs58387135
Chromosome Location chr8:8396376-8396377
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:8389200-8403000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr8:8393800-8396600 Enhancers NHDF-Ad bronchial
3 chr8:8394200-8396400 Enhancers NHLF lung
4 chr8:8394400-8396600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
5 chr8:8394800-8396400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr8:8395200-8402600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr8:8395400-8401600 Weak transcription ES-WA7 Cell Line embryonic stem cell
8 chr8:8395800-8401200 Weak transcription HSMMtube muscle
9 chr8:8395800-8401600 Weak transcription Placenta Amnion Placenta Amnion
10 chr8:8396000-8401200 Weak transcription HUVEC blood vessel
11 chr8:8396000-8401400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr8:8396000-8401600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr8:8396000-8401800 Weak transcription Placenta Placenta
14 chr8:8396000-8405000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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