Variant report

Variant rs11229624
Chromosome Location chr11:58555804-58555805
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:58554000-58556400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr11:58554000-58556800 Enhancers HMEC breast
3 chr11:58554400-58556600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr11:58554400-58557000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr11:58554800-58556600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr11:58554800-58557200 Weak transcription Skeletal Muscle Male skeletal muscle
7 chr11:58555400-58556000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr11:58555400-58556000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr11:58555400-58556000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr11:58555400-58556000 Enhancers HepG2 liver
11 chr11:58555400-58556000 Enhancers NHDF-Ad bronchial
12 chr11:58555400-58556400 Enhancers K562 blood
13 chr11:58555400-58559000 Enhancers Fetal Intestine Large intestine
14 chr11:58555600-58556000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr11:58555600-58556000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
16 chr11:58555600-58556000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
17 chr11:58555600-58556000 Enhancers Adipose Nuclei Adipose
18 chr11:58555800-58556000 Enhancers Primary T helper naive cells fromperipheralblood blood
19 chr11:58555800-58556000 Flanking Active TSS NHEK skin
20 chr11:58555800-58556400 Enhancers Pancreas Pancrea

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