Variant report

Variant rs17022431
Chromosome Location chr4:147977816-147977817
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:147971600-147978400 Weak transcription Aorta Aorta
2 chr4:147971600-147978400 Weak transcription Placenta Amnion Placenta Amnion
3 chr4:147972200-147978000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr4:147972400-147978600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr4:147973400-147978200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr4:147973800-147978000 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
7 chr4:147974000-147978200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr4:147974000-147978200 Weak transcription HMEC breast
9 chr4:147974000-147978200 Weak transcription NHEK skin
10 chr4:147975600-147978400 Enhancers Fetal Lung lung
11 chr4:147977200-147978000 Weak transcription Muscle Satellite Cultured Cells --
12 chr4:147977800-147978200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr4:147977800-147978600 Enhancers Primary T helper memory cells from peripheral blood 2 blood
14 chr4:147977800-147978600 Weak transcription Hela-S3 cervix

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