Variant report

Variant rs7117243
Chromosome Location chr11:46951309-46951310
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:46940600-46951400 Weak transcription Placenta Amnion Placenta Amnion
2 chr11:46943000-46951800 Weak transcription NHEK skin
3 chr11:46944800-46958200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr11:46946000-46951400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr11:46949600-46952400 Enhancers Duodenum Mucosa Duodenum
6 chr11:46949800-46951600 ZNF genes & repeats Fetal Intestine Small intestine
7 chr11:46950000-46952400 Enhancers Rectal Mucosa Donor 31 rectum
8 chr11:46950000-46952400 Enhancers Stomach Mucosa stomach
9 chr11:46950200-46952600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr11:46951000-46951600 Enhancers A549 lung
11 chr11:46951000-46952200 Enhancers Hela-S3 cervix
12 chr11:46951000-46952400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr11:46951000-46952400 Enhancers Fetal Intestine Large intestine
14 chr11:46951200-46952400 Enhancers Primary hematopoietic stem cells short term culture blood
15 chr11:46951200-46952400 Enhancers HepG2 liver

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