Variant report

Variant rs10775138
Chromosome Location chr15:49247983-49247984
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:49239000-49255200 Weak transcription Hela-S3 cervix
2 chr15:49246200-49248200 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr15:49246200-49249000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
4 chr15:49246400-49248400 Enhancers HMEC breast
5 chr15:49246400-49248800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr15:49246600-49248000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr15:49246800-49254000 Weak transcription Right Atrium heart
8 chr15:49247200-49250200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr15:49247600-49250000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr15:49247600-49251400 Weak transcription Left Ventricle heart
11 chr15:49247600-49252400 Weak transcription Aorta Aorta
12 chr15:49247600-49254600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr15:49247600-49254600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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