Variant report

Variant rs1477260
Chromosome Location chr14:78256818-78256819
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:78253600-78260800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr14:78253600-78261800 Weak transcription iPS-15b Cell Line embryonic stem cell
3 chr14:78253800-78266200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr14:78255200-78257000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr14:78255200-78257000 Weak transcription HepG2 liver
6 chr14:78256600-78258000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr14:78256600-78258000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr14:78256600-78258200 Enhancers Placenta Placenta
9 chr14:78256600-78258400 Enhancers Hela-S3 cervix
10 chr14:78256800-78257400 Enhancers Fetal Intestine Large intestine
11 chr14:78256800-78258000 Enhancers ES-WA7 Cell Line embryonic stem cell
12 chr14:78256800-78258000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr14:78256800-78258200 Enhancers ES-I3 Cell Line embryonic stem cell
14 chr14:78256800-78258200 Enhancers NHEK skin

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