Variant report

Variant rs74129429
Chromosome Location chr1:152224407-152224408
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:152218600-152224600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr1:152219400-152230200 Weak transcription Ovary ovary
3 chr1:152220800-152230400 Weak transcription Brain Angular Gyrus brain
4 chr1:152222200-152225600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr1:152223200-152230400 Weak transcription Stomach Smooth Muscle stomach
6 chr1:152223400-152228400 Weak transcription Fetal Adrenal Gland Adrenal Gland
7 chr1:152223600-152225400 Enhancers HMEC breast
8 chr1:152223600-152229600 Weak transcription Duodenum Smooth Muscle Duodenum
9 chr1:152223800-152225200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr1:152224000-152225400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:152224400-152224600 Enhancers Fetal Kidney kidney
12 chr1:152224400-152224800 Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr1:152224400-152225200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr1:152224400-152225200 Flanking Active TSS NHEK skin
15 chr1:152224400-152226200 Enhancers Breast Myoepithelial Primary Cells Breast

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