Variant report

Variant rs194760
Chromosome Location chr14:69212948-69212949
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:69198400-69214000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr14:69201200-69222600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr14:69202800-69224600 Weak transcription Primary T helper naive cells from peripheral blood blood
4 chr14:69203600-69213800 Weak transcription Esophagus oesophagus
5 chr14:69204200-69219200 Weak transcription Adipose Nuclei Adipose
6 chr14:69204400-69213800 Weak transcription Right Atrium heart
7 chr14:69205600-69214200 Weak transcription Spleen Spleen
8 chr14:69205600-69216200 Weak transcription Lung lung
9 chr14:69212000-69213800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr14:69212400-69213000 Enhancers HUES6 Cell Line embryonic stem cell
11 chr14:69212600-69213800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr14:69212600-69213800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr14:69212600-69215400 Weak transcription Right Ventricle heart
14 chr14:69212600-69229200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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