Variant report

Variant rs13379118
Chromosome Location chr14:66997295-66997296
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:66995600-67003600 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
2 chr14:66996400-66997400 ZNF genes & repeats Fetal Intestine Small intestine
3 chr14:66996400-66998000 Enhancers Left Ventricle heart
4 chr14:66996600-66997600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr14:66996800-66997600 Enhancers Gastric stomach
6 chr14:66996800-66997600 Enhancers GM12878-XiMat blood
7 chr14:66997000-66997400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr14:66997000-66997600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr14:66997000-66997600 Enhancers Esophagus oesophagus
10 chr14:66997000-66997600 Enhancers Right Ventricle heart
11 chr14:66997000-66997800 Enhancers NHEK skin
12 chr14:66997200-66997600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr14:66997200-66997600 Enhancers Lung lung
14 chr14:66997200-66997800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr14:66997200-66998800 Weak transcription Fetal Stomach stomach

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