Variant report

Variant rs55955608
Chromosome Location chr3:111795116-111795117
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:111791600-111796600 Weak transcription Primary T regulatory cells fromperipheralblood blood
2 chr3:111792600-111795200 Enhancers Primary T helper memory cells from peripheral blood 2 blood
3 chr3:111793200-111795400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr3:111793600-111796000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
5 chr3:111794000-111795200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr3:111794400-111795200 Enhancers Primary T cells from cord blood blood
7 chr3:111794600-111795200 Enhancers A549 lung
8 chr3:111794600-111795200 Enhancers HMEC breast
9 chr3:111794600-111795400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr3:111794600-111795800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr3:111794600-111796000 Enhancers Fetal Intestine Small intestine
12 chr3:111794600-111797600 Enhancers Fetal Thymus thymus
13 chr3:111794600-111797800 Enhancers Thymus Thymus
14 chr3:111794800-111804800 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
15 chr3:111795000-111795200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr3:111795000-111796800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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