Variant report

Variant rs58550934
Chromosome Location chr8:94919385-94919386
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:94914600-94928200 Weak transcription Right Ventricle heart
2 chr8:94916000-94919600 Enhancers Primary B cells from cord blood blood
3 chr8:94916200-94919400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr8:94916200-94919600 Enhancers Primary monocytes fromperipheralblood blood
5 chr8:94916600-94928000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr8:94917800-94923000 Weak transcription HSMMtube muscle
7 chr8:94918600-94919800 Enhancers Primary T regulatory cells fromperipheralblood blood
8 chr8:94918800-94919600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr8:94918800-94919800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr8:94918800-94921600 Weak transcription Skeletal Muscle Male skeletal muscle
11 chr8:94919000-94919400 Weak transcription Primary T helper 17 cells PMA-I stimulated --
12 chr8:94919000-94920000 ZNF genes & repeats Primary B cells from peripheral blood blood
13 chr8:94919200-94919600 ZNF genes & repeats Primary T helper cells PMA-I stimulated --
14 chr8:94919200-94919800 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr8:94919200-94919800 ZNF genes & repeats Left Ventricle heart
16 chr8:94919200-94920000 ZNF genes & repeats Monocytes-CD14+_RO01746 blood

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