Variant report

Variant rs17665188
Chromosome Location chr17:44357351-44357352
allele A/C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:44351800-44364200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
2 chr17:44353800-44364200 Weak transcription Fetal Intestine Small intestine
3 chr17:44355000-44366600 Weak transcription Fetal Stomach stomach
4 chr17:44356200-44359000 Enhancers HepG2 liver
5 chr17:44356600-44357600 Enhancers Stomach Mucosa stomach
6 chr17:44356800-44357600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr17:44356800-44358200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr17:44356800-44358200 Enhancers NHDF-Ad bronchial
9 chr17:44357000-44357400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr17:44357000-44357400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
11 chr17:44357000-44357400 Flanking Active TSS A549 lung
12 chr17:44357000-44357400 Enhancers NHEK skin
13 chr17:44357000-44357600 Enhancers Muscle Satellite Cultured Cells --
14 chr17:44357000-44357600 Enhancers Osteobl bone
15 chr17:44357000-44357800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
16 chr17:44357000-44357800 Enhancers HUVEC blood vessel
17 chr17:44357200-44357400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
18 chr17:44357200-44357600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
19 chr17:44357200-44357600 Enhancers K562 blood
20 chr17:44357200-44362000 Weak transcription HSMMtube muscle

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