Variant report

Variant rs4713579
Chromosome Location chr6:11486964-11486965
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:11480200-11491200 Weak transcription Fetal Kidney kidney
2 chr6:11483800-11495000 Weak transcription Pancreas Pancrea
3 chr6:11485400-11487000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr6:11485400-11487400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr6:11485400-11488200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr6:11485600-11488000 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr6:11485800-11487000 Enhancers Ovary ovary
8 chr6:11486000-11487000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr6:11486400-11487000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr6:11486400-11487000 Enhancers HUES64 Cell Line embryonic stem cell
11 chr6:11486400-11487000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
12 chr6:11486400-11487000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:11486600-11488000 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr6:11486800-11487000 Enhancers Lung lung
15 chr6:11486800-11487200 Weak transcription iPS-20b Cell Line embryonic stem cell
16 chr6:11486800-11496000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
17 chr6:11486800-11496800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin

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