Variant report

Variant rs4919027
Chromosome Location chr10:98265064-98265065
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:98254400-98266400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr10:98261000-98266400 Enhancers HMEC breast
3 chr10:98261600-98266200 Weak transcription Left Ventricle heart
4 chr10:98261600-98266200 Weak transcription Right Ventricle heart
5 chr10:98261600-98266600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr10:98261800-98268400 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr10:98262800-98266200 Weak transcription Esophagus oesophagus
8 chr10:98263200-98265200 Weak transcription GM12878-XiMat blood
9 chr10:98264400-98266600 Enhancers NHEK skin
10 chr10:98264600-98265600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr10:98264800-98266400 Enhancers Breast Myoepithelial Primary Cells Breast
12 chr10:98264800-98266400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr10:98264800-98266400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr10:98265000-98265200 Enhancers iPS-20b Cell Line embryonic stem cell
15 chr10:98265000-98265200 Enhancers Skeletal Muscle Male skeletal muscle
16 chr10:98265000-98265800 Enhancers Fetal Heart heart

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