Variant report

Variant rs7853718
Chromosome Location chr9:16749884-16749885
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:16745400-16752400 Weak transcription Colon Smooth Muscle Colon
2 chr9:16745400-16758000 Weak transcription Ovary ovary
3 chr9:16745400-16774800 Weak transcription Osteobl bone
4 chr9:16745600-16750600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr9:16745600-16752200 Weak transcription NHDF-Ad bronchial
6 chr9:16745600-16766200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr9:16748000-16752200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr9:16748200-16752200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:16748600-16750000 Enhancers HUES48 Cell Line embryonic stem cell
10 chr9:16749000-16750600 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr9:16749000-16750800 Enhancers HUES64 Cell Line embryonic stem cell
12 chr9:16749200-16750000 Enhancers ES-I3 Cell Line embryonic stem cell
13 chr9:16749200-16750000 Enhancers iPS-15b Cell Line embryonic stem cell
14 chr9:16749600-16750000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
15 chr9:16749600-16750200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
16 chr9:16749600-16750400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
17 chr9:16749600-16755000 Weak transcription iPS-20b Cell Line embryonic stem cell

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