Variant report

Variant rs10093649
Chromosome Location chr8:125872234-125872235
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:125869400-125872600 Weak transcription NHDF-Ad bronchial
2 chr8:125869400-125873400 Weak transcription Right Atrium heart
3 chr8:125869400-125876400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr8:125869600-125872600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr8:125869600-125873600 Weak transcription Right Ventricle heart
6 chr8:125869800-125873200 Weak transcription Ovary ovary
7 chr8:125869800-125873200 Weak transcription K562 blood
8 chr8:125869800-125873400 Weak transcription Left Ventricle heart
9 chr8:125869800-125874000 Weak transcription Osteobl bone
10 chr8:125869800-125874400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr8:125869800-125878200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr8:125870000-125873400 Weak transcription Fetal Adrenal Gland Adrenal Gland
13 chr8:125870200-125874000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr8:125870200-125879000 Weak transcription Fetal Heart heart
15 chr8:125870600-125879200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr8:125871000-125885200 Weak transcription Esophagus oesophagus
17 chr8:125871200-125873400 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr8:125871200-125878000 Weak transcription NHEK skin
19 chr8:125871600-125878000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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