Variant report

Variant rs11647813
Chromosome Location chr16:12705536-12705537
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:12703400-12706400 Enhancers HepG2 liver
2 chr16:12703400-12706800 Enhancers Liver Liver
3 chr16:12703800-12706800 Enhancers K562 blood
4 chr16:12703800-12708000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr16:12704000-12708800 Enhancers Placenta Placenta
6 chr16:12704200-12708400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr16:12704400-12705600 Enhancers A549 lung
8 chr16:12704400-12707400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr16:12704400-12707400 Enhancers Stomach Mucosa stomach
10 chr16:12704600-12708200 Enhancers NHEK skin
11 chr16:12704800-12705800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr16:12704800-12707200 Enhancers ES-I3 Cell Line embryonic stem cell
13 chr16:12704800-12709400 Enhancers Fetal Intestine Large intestine
14 chr16:12705000-12705600 Enhancers iPS-20b Cell Line embryonic stem cell
15 chr16:12705000-12706400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr16:12705000-12706400 Weak transcription HMEC breast
17 chr16:12705000-12707800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
18 chr16:12705000-12709000 Enhancers Fetal Intestine Small intestine
19 chr16:12705400-12705600 Enhancers iPS-18 Cell Line embryonic stem cell

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