Variant report

Variant rs12218376
Chromosome Location chr10:44389430-44389431
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:44360000-44392200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr10:44387200-44389600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
3 chr10:44387800-44394600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr10:44388600-44389600 Weak transcription Fetal Stomach stomach
5 chr10:44388800-44391400 Weak transcription Fetal Muscle Leg muscle
6 chr10:44388800-44393800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr10:44388800-44393800 Weak transcription Right Atrium heart
8 chr10:44388800-44394000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
9 chr10:44388800-44394000 Weak transcription Left Ventricle heart
10 chr10:44388800-44394200 Weak transcription Osteobl bone
11 chr10:44388800-44397600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr10:44389000-44390400 Weak transcription NHDF-Ad bronchial
13 chr10:44389000-44394200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr10:44389000-44394800 Weak transcription Fetal Kidney kidney
15 chr10:44389400-44390800 Weak transcription Fetal Heart heart

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