Variant report

Variant rs374576827
Chromosome Location chr21:44949592-44949593
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:44943400-44956800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr21:44943600-44952400 Weak transcription HMEC breast
3 chr21:44943600-44952600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr21:44945400-44949600 Strong transcription HSMMtube muscle
5 chr21:44945600-44951400 Weak transcription Placenta Amnion Placenta Amnion
6 chr21:44946800-44951600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr21:44946800-44962800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr21:44947600-44949800 Strong transcription NHEK skin
9 chr21:44947800-44949600 Strong transcription HSMM muscle
10 chr21:44949000-44949600 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr21:44949400-44949600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr21:44949400-44949800 Strong transcription Breast Myoepithelial Primary Cells Breast

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