Variant report

Variant rs11854103
Chromosome Location chr15:40442099-40442100
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:40428600-40442200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr15:40437400-40442200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr15:40438400-40442200 Weak transcription Hela-S3 cervix
4 chr15:40438400-40446800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr15:40438600-40442200 Weak transcription NH-A brain
6 chr15:40438800-40442200 Weak transcription A549 lung
7 chr15:40438800-40442200 Weak transcription HSMM muscle
8 chr15:40438800-40446800 Weak transcription Placenta Amnion Placenta Amnion
9 chr15:40440200-40446800 Weak transcription Pancreas Pancrea
10 chr15:40441800-40445000 Enhancers HMEC breast
11 chr15:40441800-40445200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr15:40441800-40445200 Enhancers NHEK skin
13 chr15:40442000-40442200 Enhancers HSMMtube muscle
14 chr15:40442000-40443200 Enhancers Cortex derived primary cultured neurospheres brain
15 chr15:40442000-40443400 Enhancers Brain Germinal Matrix brain
16 chr15:40442000-40443400 Enhancers Fetal Muscle Leg muscle
17 chr15:40442000-40444400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr15:40442000-40445200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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