Variant report

Variant rs6135333
Chromosome Location chr20:15026392-15026393
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:15020200-15027400 Weak transcription Fetal Intestine Small intestine
2 chr20:15024000-15029000 Enhancers Fetal Thymus thymus
3 chr20:15025000-15026800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr20:15025000-15027600 Enhancers Dnd41 blood
5 chr20:15025200-15026600 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr20:15025200-15026800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr20:15025200-15026800 Enhancers HMEC breast
8 chr20:15025600-15026800 Enhancers NHEK skin
9 chr20:15025800-15026600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr20:15025800-15026800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr20:15026000-15026800 Enhancers Thymus Thymus
12 chr20:15026000-15027000 Weak transcription Ovary ovary
13 chr20:15026200-15027600 Weak transcription Fetal Kidney kidney
14 chr20:15026200-15029800 Weak transcription Fetal Heart heart

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