Variant report

Variant rs10261725
Chromosome Location chr7:84627231-84627232
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:84625800-84628600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr7:84625800-84630200 Weak transcription Fetal Brain Male brain
3 chr7:84626200-84628200 Weak transcription Fetal Lung lung
4 chr7:84626400-84639800 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr7:84626800-84627400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr7:84626800-84627400 Enhancers HUVEC blood vessel
7 chr7:84626800-84627600 Enhancers HUES6 Cell Line embryonic stem cell
8 chr7:84627000-84627600 Enhancers HUES64 Cell Line embryonic stem cell
9 chr7:84627000-84628400 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr7:84627000-84632200 Enhancers HUES48 Cell Line embryonic stem cell
11 chr7:84627200-84627600 Weak transcription Pancreatic Islets Pancreatic Islet
12 chr7:84627200-84628200 Weak transcription ES-I3 Cell Line embryonic stem cell
13 chr7:84627200-84632800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr7:84627200-84633800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
15 chr7:84627200-84633800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
16 chr7:84627200-84636800 Weak transcription Fetal Stomach stomach

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