Variant report

Variant rs565086642
Chromosome Location chr1:242620367-242620368
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:242611000-242632200 Weak transcription HMEC breast
2 chr1:242613200-242621600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr1:242613400-242640400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr1:242615600-242635400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:242616200-242651400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:242618400-242620600 Enhancers HUES48 Cell Line embryonic stem cell
7 chr1:242619600-242623000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr1:242619600-242623600 Weak transcription Placenta Placenta
9 chr1:242619800-242620400 Enhancers iPS-20b Cell Line embryonic stem cell
10 chr1:242620200-242620400 Bivalent Enhancer Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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