Variant report

Variant rs10757253
Chromosome Location chr9:21772267-21772268
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:21765400-21772600 Weak transcription HSMM muscle
2 chr9:21770400-21772800 Enhancers NHLF lung
3 chr9:21770400-21773400 Enhancers Stomach Mucosa stomach
4 chr9:21770600-21775800 Weak transcription Primary T helper cells PMA-I stimulated --
5 chr9:21770800-21773000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr9:21771400-21773400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr9:21771600-21777000 Weak transcription Osteobl bone
8 chr9:21771800-21773400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr9:21771800-21776000 Weak transcription Primary monocytes fromperipheralblood blood
10 chr9:21771800-21776000 Weak transcription Monocytes-CD14+_RO01746 blood
11 chr9:21771800-21776400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
12 chr9:21771800-21776800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr9:21772000-21772400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr9:21772000-21776200 Weak transcription HMEC breast
15 chr9:21772000-21776400 Weak transcription Hela-S3 cervix
16 chr9:21772000-21777200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr9:21772000-21777200 Weak transcription NHDF-Ad bronchial
18 chr9:21772000-21777400 Weak transcription NHEK skin
19 chr9:21772200-21777200 Weak transcription Muscle Satellite Cultured Cells --

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