Variant report

Variant rs6681778
Chromosome Location chr1:209276755-209276756
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:209270200-209279200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:209270600-209279000 Weak transcription HSMM muscle
3 chr1:209273800-209281800 Enhancers Fetal Brain Female brain
4 chr1:209273800-209282200 Enhancers Fetal Brain Male brain
5 chr1:209274600-209277200 Enhancers Brain Germinal Matrix brain
6 chr1:209274800-209279200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
7 chr1:209275800-209277000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr1:209275800-209279000 Weak transcription HUES6 Cell Line embryonic stem cell
9 chr1:209276000-209279000 Weak transcription iPS-18 Cell Line embryonic stem cell
10 chr1:209276200-209277600 Enhancers HSMMtube muscle
11 chr1:209276400-209277200 Flanking Active TSS GM12878-XiMat blood
12 chr1:209276600-209276800 Enhancers Duodenum Mucosa Duodenum
13 chr1:209276600-209277200 Enhancers Fetal Muscle Leg muscle

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