Variant report

Variant rs60531578
Chromosome Location chr11:15894499-15894500
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:15890400-15897000 Weak transcription Fetal Intestine Small intestine
2 chr11:15891800-15894600 Enhancers Cortex derived primary cultured neurospheres brain
3 chr11:15892000-15894800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
4 chr11:15892600-15894600 Enhancers H1 Cell Line embryonic stem cell
5 chr11:15893000-15896000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr11:15893200-15895800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
7 chr11:15893600-15914000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr11:15894000-15895800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr11:15894000-15897000 Weak transcription HUES64 Cell Line embryonic stem cell
10 chr11:15894000-15897600 Weak transcription H9 Cell Line embryonic stem cell
11 chr11:15894200-15897800 Weak transcription HUES6 Cell Line embryonic stem cell
12 chr11:15894400-15895200 Weak transcription ES-I3 Cell Line embryonic stem cell
13 chr11:15894400-15897000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr11:15894400-15897600 Weak transcription iPS-18 Cell Line embryonic stem cell

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