Variant report

Variant rs73907487
Chromosome Location chr21:46822921-46822922
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46807800-46824400 Weak transcription Right Atrium heart
2 chr21:46822000-46823800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
3 chr21:46822200-46823200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr21:46822200-46824000 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr21:46822200-46824200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
6 chr21:46822200-46824400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr21:46822400-46824200 Enhancers HMEC breast
8 chr21:46822600-46823000 Enhancers NHEK skin
9 chr21:46822600-46823400 Enhancers ES-WA7 Cell Line embryonic stem cell
10 chr21:46822600-46824000 Enhancers HUES6 Cell Line embryonic stem cell
11 chr21:46822600-46824000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
12 chr21:46822600-46824600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr21:46822800-46823800 Weak transcription Ovary ovary
14 chr21:46822800-46824000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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