Variant report

Variant rs2228946
Chromosome Location chr7:116918085-116918086
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:116909600-116920400 Weak transcription Placenta Amnion Placenta Amnion
2 chr7:116914600-116918200 Weak transcription Placenta Placenta
3 chr7:116915000-116919600 Strong transcription Fetal Lung lung
4 chr7:116915400-116918200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr7:116915400-116920000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr7:116915400-116920000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr7:116915400-116920000 Weak transcription NHLF lung
8 chr7:116915800-116920000 Weak transcription Right Atrium heart
9 chr7:116917800-116919600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr7:116918000-116918200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
11 chr7:116918000-116921800 Weak transcription NHDF-Ad bronchial

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