Variant report

Variant rs10107531
Chromosome Location chr8:49064349-49064350
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49051800-49065800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr8:49056200-49066000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr8:49058000-49064800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr8:49061800-49064400 Enhancers HMEC breast
5 chr8:49062000-49064400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr8:49062200-49064400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr8:49062400-49064400 Enhancers Fetal Intestine Large intestine
8 chr8:49063000-49064400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr8:49063200-49064400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr8:49064200-49065400 Weak transcription HepG2 liver
11 chr8:49064200-49067800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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