Variant report

Variant rs41306336
Chromosome Location chr10:18295865-18295866
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:18294200-18296000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr10:18294600-18296000 Enhancers H9 Cell Line embryonic stem cell
3 chr10:18294800-18297000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr10:18295200-18296000 Enhancers Hela-S3 cervix
5 chr10:18295200-18298400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
6 chr10:18295200-18299400 Enhancers Cortex derived primary cultured neurospheres brain
7 chr10:18295400-18298400 Weak transcription NH-A brain
8 chr10:18295400-18298400 Weak transcription Osteobl bone
9 chr10:18295400-18298800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr10:18295600-18296400 Enhancers Brain Anterior Caudate brain
11 chr10:18295600-18296800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
12 chr10:18295600-18298800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr10:18295600-18298800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr10:18295800-18298600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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