Variant report

Variant rs4715962
Chromosome Location chr6:15068392-15068393
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:15043800-15077400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr6:15058200-15074400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr6:15061200-15069800 Enhancers Primary monocytes fromperipheralblood blood
4 chr6:15065200-15068600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
5 chr6:15067200-15076600 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr6:15067400-15068600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr6:15067400-15073200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr6:15067400-15076600 Weak transcription ES-I3 Cell Line embryonic stem cell
9 chr6:15067600-15068800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr6:15067600-15068800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr6:15067600-15072600 Weak transcription Stomach Mucosa stomach
12 chr6:15067600-15076200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr6:15067800-15069200 Enhancers Monocytes-CD14+_RO01746 blood
14 chr6:15067800-15071600 Weak transcription K562 blood
15 chr6:15067800-15073200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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