Variant report

Variant rs2288778
Chromosome Location chr5:150920566-150920567
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:150889000-150932600 Weak transcription Skeletal Muscle Male skeletal muscle
2 chr5:150901800-150935600 Weak transcription Fetal Intestine Small intestine
3 chr5:150905800-150934000 Weak transcription Adipose Nuclei Adipose
4 chr5:150908200-150948000 Strong transcription HMEC breast
5 chr5:150908400-150933400 Strong transcription Breast Myoepithelial Primary Cells Breast
6 chr5:150908400-150944000 Strong transcription NHEK skin
7 chr5:150909200-150942400 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr5:150911600-150942800 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr5:150914200-150935600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr5:150914200-150938600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr5:150917600-150920600 Strong transcription Esophagus oesophagus
12 chr5:150918200-150945400 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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