Variant report

Variant rs13433684
Chromosome Location chr3:100426280-100426281
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100422200-100427400 Weak transcription A549 lung
2 chr3:100422200-100427400 Weak transcription GM12878-XiMat blood
3 chr3:100422600-100427200 Weak transcription Fetal Intestine Small intestine
4 chr3:100424600-100426400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr3:100424600-100427400 Weak transcription Esophagus oesophagus
6 chr3:100424800-100426600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr3:100425200-100427400 Weak transcription Placenta Amnion Placenta Amnion
8 chr3:100425400-100427400 Weak transcription HSMMtube muscle
9 chr3:100425600-100427400 Weak transcription K562 blood
10 chr3:100425800-100427000 Weak transcription NHEK skin
11 chr3:100425800-100427200 Weak transcription HMEC breast
12 chr3:100425800-100427400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr3:100425800-100427600 Weak transcription Aorta Aorta
14 chr3:100425800-100427600 Enhancers Fetal Intestine Large intestine

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