Variant report

Variant rs4858506
Chromosome Location chr3:23382060-23382061
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:23367400-23391400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr3:23368000-23391000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr3:23372200-23383400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr3:23373200-23382200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr3:23379000-23383600 Weak transcription Psoas Muscle Psoas
6 chr3:23380600-23382200 Weak transcription Colon Smooth Muscle Colon
7 chr3:23380800-23382400 Enhancers Primary B cells from cord blood blood
8 chr3:23380800-23389400 Weak transcription HUES64 Cell Line embryonic stem cell
9 chr3:23381200-23382200 Weak transcription Small Intestine intestine
10 chr3:23381600-23383000 Enhancers HUES48 Cell Line embryonic stem cell
11 chr3:23381800-23383000 Enhancers Duodenum Smooth Muscle Duodenum
12 chr3:23382000-23382600 Enhancers Monocytes-CD14+_RO01746 blood
13 chr3:23382000-23383600 Flanking Active TSS GM12878-XiMat blood
14 chr3:23382000-23384600 Enhancers Primary B cells from peripheral blood blood

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