Variant report

Variant rs9299985
Chromosome Location chr11:3597557-3597558
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:3595400-3602000 Weak transcription Right Atrium heart
2 chr11:3596800-3597600 Enhancers ES-I3 Cell Line embryonic stem cell
3 chr11:3596800-3597600 Enhancers H9 Cell Line embryonic stem cell
4 chr11:3596800-3597600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
5 chr11:3596800-3597800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr11:3596800-3598000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr11:3596800-3598200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr11:3597400-3597600 Enhancers H1 Cell Line embryonic stem cell
9 chr11:3597400-3597600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr11:3597400-3597600 Enhancers HUES48 Cell Line embryonic stem cell
11 chr11:3597400-3597600 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr11:3597400-3597800 Enhancers HUES6 Cell Line embryonic stem cell
13 chr11:3597400-3598000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
14 chr11:3597400-3598000 Genic enhancers Fetal Intestine Small intestine
15 chr11:3597400-3598000 Enhancers Placenta Amnion Placenta Amnion

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