Variant report

Variant rs10179054
Chromosome Location chr2:31506424-31506425
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:31486600-31510000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr2:31492400-31507800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr2:31492800-31510600 Weak transcription Aorta Aorta
4 chr2:31495800-31509800 Weak transcription Esophagus oesophagus
5 chr2:31497000-31510400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr2:31504600-31512800 Enhancers Placenta Placenta
7 chr2:31505800-31508200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr2:31506000-31507000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr2:31506200-31509000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr2:31506200-31510000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr2:31506400-31508400 Weak transcription Fetal Adrenal Gland Adrenal Gland
12 chr2:31506400-31508800 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr2:31506400-31508800 Weak transcription HUVEC blood vessel

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