Variant report

Variant rs17046858
Chromosome Location chr4:166530760-166530761
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:166525400-166533800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr4:166525600-166532000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
3 chr4:166525600-166539200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr4:166526200-166531600 Weak transcription Rectal Smooth Muscle rectum
5 chr4:166528000-166532200 Weak transcription Adipose Nuclei Adipose
6 chr4:166530400-166536000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr4:166530600-166531000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
8 chr4:166530600-166531000 Enhancers iPS-20b Cell Line embryonic stem cell
9 chr4:166530600-166531800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr4:166530600-166531800 Enhancers iPS-15b Cell Line embryonic stem cell
11 chr4:166530600-166532600 Enhancers Colon Smooth Muscle Colon
12 chr4:166530600-166534200 Enhancers HUES48 Cell Line embryonic stem cell
13 chr4:166530600-166535400 Enhancers iPS-18 Cell Line embryonic stem cell

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