Variant report

Variant rs459466
Chromosome Location chr21:28178908-28178909
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:28170800-28181000 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr21:28174000-28185400 Weak transcription HSMMtube muscle
3 chr21:28174600-28187800 Weak transcription Osteobl bone
4 chr21:28177800-28179400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
5 chr21:28177800-28186800 Weak transcription NHLF lung
6 chr21:28178200-28179200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr21:28178200-28183000 Weak transcription Fetal Stomach stomach
8 chr21:28178200-28185800 Weak transcription Ovary ovary
9 chr21:28178600-28179200 Enhancers NHDF-Ad bronchial
10 chr21:28178800-28179400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr21:28178800-28179400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr21:28178800-28179800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr21:28178800-28179800 Enhancers Muscle Satellite Cultured Cells --
14 chr21:28178800-28179800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr21:28178800-28179800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr21:28178800-28179800 Enhancers HMEC breast
17 chr21:28178800-28179800 Enhancers NHEK skin
18 chr21:28178800-28180000 Enhancers Hela-S3 cervix
19 chr21:28178800-28180200 Enhancers Dnd41 blood

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