Variant report

Variant rs9290170
Chromosome Location chr3:100425460-100425461
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100422200-100425800 Weak transcription Fetal Intestine Large intestine
2 chr3:100422200-100427400 Weak transcription A549 lung
3 chr3:100422200-100427400 Weak transcription GM12878-XiMat blood
4 chr3:100422600-100427200 Weak transcription Fetal Intestine Small intestine
5 chr3:100424600-100426400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr3:100424600-100427400 Weak transcription Esophagus oesophagus
7 chr3:100424800-100425800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr3:100424800-100425800 Enhancers HMEC breast
9 chr3:100424800-100425800 Enhancers NHEK skin
10 chr3:100424800-100426600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr3:100425000-100425600 Enhancers K562 blood
12 chr3:100425200-100427400 Weak transcription Placenta Amnion Placenta Amnion
13 chr3:100425400-100427400 Weak transcription HSMMtube muscle

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