Variant report

Variant rs194762
Chromosome Location chr14:69211893-69211894
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr14:69209200-69212000 Weak transcription Fetal Thymus thymus
10 chr14:69210200-69212200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr14:69211400-69212000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
12 chr14:69211600-69212000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
13 chr14:69211600-69212800 Enhancers Cortex derived primary cultured neurospheres brain

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