Variant report

Variant rs7147192
Chromosome Location chr14:66996985-66996986
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:66977600-66997200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr14:66995600-67003600 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
3 chr14:66996400-66997400 ZNF genes & repeats Fetal Intestine Small intestine
4 chr14:66996400-66998000 Enhancers Left Ventricle heart
5 chr14:66996600-66997200 Strong transcription Fetal Stomach stomach
6 chr14:66996600-66997600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr14:66996800-66997600 Enhancers Gastric stomach
8 chr14:66996800-66997600 Enhancers GM12878-XiMat blood

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