Variant report

Variant rs11994576
Chromosome Location chr8:125873292-125873293
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:125869400-125873400 Weak transcription Right Atrium heart
2 chr8:125869400-125876400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr8:125869600-125873600 Weak transcription Right Ventricle heart
4 chr8:125869800-125873400 Weak transcription Left Ventricle heart
5 chr8:125869800-125874000 Weak transcription Osteobl bone
6 chr8:125869800-125874400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr8:125869800-125878200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr8:125870000-125873400 Weak transcription Fetal Adrenal Gland Adrenal Gland
9 chr8:125870200-125874000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr8:125870200-125879000 Weak transcription Fetal Heart heart
11 chr8:125870600-125879200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr8:125871000-125885200 Weak transcription Esophagus oesophagus
13 chr8:125871200-125873400 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr8:125871200-125878000 Weak transcription NHEK skin
15 chr8:125871600-125878000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr8:125872600-125875400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr8:125873000-125874600 Weak transcription NHDF-Ad bronchial
18 chr8:125873200-125873800 Enhancers K562 blood
19 chr8:125873200-125874600 Enhancers Ovary ovary

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