Variant report

Variant rs34114148
Chromosome Location chr5:53737701-53737702
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:53733600-53738600 Enhancers Fetal Intestine Large intestine
2 chr5:53735000-53742600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr5:53735600-53738000 Enhancers Primary T helper cells fromperipheralblood blood
4 chr5:53735800-53738000 Enhancers Fetal Thymus thymus
5 chr5:53735800-53739200 Enhancers Placenta Placenta
6 chr5:53736000-53738200 Enhancers Thymus Thymus
7 chr5:53736200-53738200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr5:53736200-53739400 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr5:53736600-53738600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr5:53736800-53737800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr5:53736800-53738600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr5:53736800-53738600 Enhancers NHEK skin
13 chr5:53736800-53739200 Enhancers Placenta Amnion Placenta Amnion
14 chr5:53737400-53737800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr5:53737400-53737800 Weak transcription Primary T cells from cord blood blood
16 chr5:53737600-53738000 Weak transcription GM12878-XiMat blood
17 chr5:53737600-53738600 Enhancers HMEC breast

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