Variant report

Variant rs544487045
Chromosome Location chr12:116852225-116852226
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:116842400-116853400 Weak transcription HUES6 Cell Line embryonic stem cell
2 chr12:116844800-116862400 Weak transcription Placenta Amnion Placenta Amnion
3 chr12:116847000-116853000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr12:116848000-116853200 Weak transcription Spleen Spleen
5 chr12:116848800-116852800 Weak transcription Fetal Brain Male brain
6 chr12:116848800-116853200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr12:116849000-116853200 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr12:116849000-116853800 Weak transcription A549 lung
9 chr12:116849000-116854000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr12:116849000-116858200 Weak transcription Colon Smooth Muscle Colon
11 chr12:116849200-116854000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr12:116849200-116858000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
13 chr12:116849600-116853600 Weak transcription Fetal Muscle Trunk muscle
14 chr12:116849800-116854000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
15 chr12:116850000-116860600 Weak transcription NHDF-Ad bronchial
16 chr12:116850400-116852800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
17 chr12:116850600-116853000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell

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