Variant report

Variant rs3923672
Chromosome Location chr2:21136225-21136226
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:21131200-21136400 Enhancers Fetal Adrenal Gland Adrenal Gland
2 chr2:21131600-21136400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr2:21131600-21136600 Weak transcription NHEK skin
4 chr2:21131800-21137000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:21133000-21136400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr2:21133400-21136800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr2:21133400-21149400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr2:21135200-21139200 Weak transcription Colon Smooth Muscle Colon
9 chr2:21135200-21139400 Weak transcription Rectal Smooth Muscle rectum
10 chr2:21135600-21139400 Weak transcription Ovary ovary

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