Variant report

Variant rs10988791
Chromosome Location chr9:102151315-102151316
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:102148400-102151400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr9:102148400-102151400 Weak transcription Esophagus oesophagus
3 chr9:102148400-102151400 Weak transcription NH-A brain
4 chr9:102148400-102154200 Weak transcription Left Ventricle heart
5 chr9:102148400-102161800 Weak transcription Right Ventricle heart
6 chr9:102148600-102153800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr9:102148800-102151400 Weak transcription Placenta Placenta
8 chr9:102148800-102151600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
9 chr9:102148800-102151600 Weak transcription NHLF lung
10 chr9:102149600-102151400 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr9:102149800-102151600 Weak transcription HUVEC blood vessel
12 chr9:102150000-102151400 Weak transcription NHDF-Ad bronchial
13 chr9:102150000-102151600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr9:102151000-102152000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr9:102151000-102152200 Enhancers HMEC breast
16 chr9:102151200-102152000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
17 chr9:102151200-102152200 Enhancers NHEK skin

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