Variant report

Variant rs2300009
Chromosome Location chr7:107920134-107920135
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:107887400-107925000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
2 chr7:107907200-107923400 Weak transcription Fetal Brain Male brain
3 chr7:107907400-107923400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:107907800-107925000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr7:107911400-107922000 Weak transcription Cortex derived primary cultured neurospheres brain
6 chr7:107912600-107923000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr7:107917200-107922600 Weak transcription Right Atrium heart
8 chr7:107918400-107935000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr7:107919000-107920200 Weak transcription Pancreas Pancrea
10 chr7:107919000-107920600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr7:107919200-107924800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr7:107919400-107920400 Weak transcription A549 lung
13 chr7:107919400-107924200 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr7:107919400-107926400 Enhancers HUVEC blood vessel
15 chr7:107920000-107920600 Enhancers K562 blood

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