Variant report

Variant rs6079710
Chromosome Location chr20:15203893-15203894
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:15199200-15205000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr20:15199800-15205200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
3 chr20:15200000-15204600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr20:15200200-15204000 Enhancers H9 Cell Line embryonic stem cell
5 chr20:15200200-15204000 Enhancers iPS-20b Cell Line embryonic stem cell
6 chr20:15200600-15204000 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr20:15200600-15204200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
8 chr20:15200800-15204200 Enhancers HUVEC blood vessel
9 chr20:15201800-15205600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr20:15202200-15217400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr20:15203200-15204200 Enhancers Fetal Brain Male brain
12 chr20:15203400-15204000 Enhancers HUES6 Cell Line embryonic stem cell
13 chr20:15203400-15204200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
14 chr20:15203600-15204000 Enhancers ES-I3 Cell Line embryonic stem cell
15 chr20:15203600-15204200 Flanking Active TSS Brain Germinal Matrix brain
16 chr20:15203800-15204000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
17 chr20:15203800-15204000 Flanking Active TSS Brain Anterior Caudate brain

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