Variant report

Variant rs10209193
Chromosome Location chr2:37407630-37407631
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:37406200-37407800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr2:37406600-37408000 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr2:37406800-37407800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr2:37406800-37407800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr2:37407000-37407800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr2:37407000-37408000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr2:37407000-37408000 Enhancers Adipose Nuclei Adipose
8 chr2:37407200-37408000 Bivalent Enhancer IMR90 fetal lung fibroblasts Cell Line lung
9 chr2:37407200-37409600 Enhancers HUES48 Cell Line embryonic stem cell
10 chr2:37407400-37408400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr2:37407400-37408400 Weak transcription iPS-20b Cell Line embryonic stem cell
12 chr2:37407400-37409600 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr2:37407400-37409800 Enhancers iPS-15b Cell Line embryonic stem cell
14 chr2:37407400-37410000 Enhancers HUES6 Cell Line embryonic stem cell

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