Variant report

Variant rs16925389
Chromosome Location chr10:25405627-25405628
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:25392400-25414200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr10:25402600-25409600 Weak transcription Pancreas Pancrea
3 chr10:25403200-25405800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr10:25403200-25406400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr10:25403400-25405800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr10:25403400-25406200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr10:25403400-25406800 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr10:25404600-25406200 Enhancers HUES64 Cell Line embryonic stem cell
9 chr10:25404600-25406200 Enhancers iPS-20b Cell Line embryonic stem cell
10 chr10:25404800-25405800 Enhancers H1 Cell Line embryonic stem cell
11 chr10:25404800-25406000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr10:25404800-25406200 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr10:25405200-25406600 Weak transcription K562 blood
14 chr10:25405400-25406000 Enhancers HUES48 Cell Line embryonic stem cell
15 chr10:25405600-25406000 Enhancers H9 Cell Line embryonic stem cell
16 chr10:25405600-25406800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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