Variant report

Variant rs11118897
Chromosome Location chr1:222097042-222097043
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:222075200-222097400 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr1:222081200-222097600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr1:222086000-222097600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr1:222087600-222099200 Weak transcription Primary monocytes fromperipheralblood blood
5 chr1:222094800-222099200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr1:222095400-222117800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:222095800-222097600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr1:222095800-222097600 Weak transcription Osteobl bone
9 chr1:222097000-222097400 Weak transcription NHDF-Ad bronchial
10 chr1:222097000-222098200 Enhancers Muscle Satellite Cultured Cells --

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