Variant report

Variant rs60638976
Chromosome Location chr2:31507995-31507996
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr2:31492800-31510600 Weak transcription Aorta Aorta
3 chr2:31495800-31509800 Weak transcription Esophagus oesophagus
4 chr2:31497000-31510400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr2:31504600-31512800 Enhancers Placenta Placenta
6 chr2:31505800-31508200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr2:31506200-31509000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr2:31506200-31510000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr2:31506400-31508400 Weak transcription Fetal Adrenal Gland Adrenal Gland
10 chr2:31506400-31508800 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr2:31506400-31508800 Weak transcription HUVEC blood vessel
12 chr2:31507400-31511000 Weak transcription HUES6 Cell Line embryonic stem cell
13 chr2:31507600-31510200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr2:31507800-31510600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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