Variant report

Variant rs4928083
Chromosome Location chr3:100421065-100421066
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100415800-100424600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr3:100417000-100423600 Weak transcription Esophagus oesophagus
3 chr3:100418400-100421400 Weak transcription Fetal Intestine Large intestine
4 chr3:100418600-100421400 Weak transcription Fetal Intestine Small intestine
5 chr3:100418800-100425000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr3:100420200-100421600 Enhancers HMEC breast
7 chr3:100420400-100421600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr3:100420400-100421600 Enhancers NHEK skin
9 chr3:100420400-100422200 Enhancers K562 blood
10 chr3:100420800-100421600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr3:100421000-100421200 Enhancers GM12878-XiMat blood

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