Variant report

Variant rs188850238
Chromosome Location chr5:17411602-17411603
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:17403000-17413000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr5:17407000-17413000 Weak transcription Stomach Mucosa stomach
3 chr5:17407200-17411800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr5:17407200-17411800 Weak transcription HMEC breast
5 chr5:17407200-17412200 Weak transcription NH-A brain
6 chr5:17407800-17413200 Weak transcription Hela-S3 cervix
7 chr5:17411200-17412400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr5:17411200-17416000 Enhancers Fetal Brain Male brain
9 chr5:17411400-17412000 Weak transcription H9 Cell Line embryonic stem cell
10 chr5:17411400-17412200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr5:17411400-17412600 Enhancers NHEK skin
12 chr5:17411600-17411800 Enhancers iPS-15b Cell Line embryonic stem cell
13 chr5:17411600-17411800 Enhancers Monocytes-CD14+_RO01746 blood
14 chr5:17411600-17412800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
15 chr5:17411600-17413000 Enhancers Primary neutrophils fromperipheralblood blood

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