Variant report

Variant rs1880579
Chromosome Location chr7:70390228-70390229
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:70373200-70400200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr7:70388600-70391600 Weak transcription Fetal Kidney kidney
3 chr7:70388800-70390400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr7:70388800-70390600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr7:70388800-70390600 Weak transcription Fetal Intestine Large intestine
6 chr7:70390000-70390800 Enhancers ES-I3 Cell Line embryonic stem cell
7 chr7:70390000-70390800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr7:70390000-70390800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
9 chr7:70390200-70390600 Enhancers HUES6 Cell Line embryonic stem cell
10 chr7:70390200-70390600 Enhancers HUES64 Cell Line embryonic stem cell
11 chr7:70390200-70390600 Enhancers iPS-15b Cell Line embryonic stem cell
12 chr7:70390200-70390600 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr7:70390200-70390800 Enhancers H1 Cell Line embryonic stem cell
14 chr7:70390200-70390800 Enhancers HUES48 Cell Line embryonic stem cell
15 chr7:70390200-70391000 Enhancers iPS-20b Cell Line embryonic stem cell

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