Variant report

Variant rs12294098
Chromosome Location chr11:67579791-67579792
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:67574200-67593400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr11:67579200-67579800 Bivalent Enhancer Brain Germinal Matrix brain
3 chr11:67579200-67579800 Enhancers Fetal Brain Female brain
4 chr11:67579400-67579800 Active TSS Breast Myoepithelial Primary Cells Breast
5 chr11:67579400-67579800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr11:67579400-67579800 Bivalent Enhancer Rectal Mucosa Donor 29 rectum
7 chr11:67579400-67579800 Bivalent/Poised TSS Hela-S3 cervix
8 chr11:67579400-67580000 Enhancers Rectal Mucosa Donor 31 rectum
9 chr11:67579600-67579800 Enhancers HUES48 Cell Line embryonic stem cell
10 chr11:67579600-67579800 Enhancers HUES6 Cell Line embryonic stem cell
11 chr11:67579600-67579800 Bivalent/Poised TSS Cortex derived primary cultured neurospheres brain
12 chr11:67579600-67580000 Enhancers Lung lung
13 chr11:67579600-67580000 Bivalent Enhancer A549 lung
14 chr11:67579600-67580200 Enhancers Left Ventricle heart
15 chr11:67579600-67580800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain

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