Variant report

Variant rs548274201
Chromosome Location chr7:124894806-124894807
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:124887400-124898000 Weak transcription H9 Cell Line embryonic stem cell
2 chr7:124891000-124895600 Weak transcription ES-WA7 Cell Line embryonic stem cell
3 chr7:124892400-124896000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr7:124892600-124896000 Genic enhancers HUES6 Cell Line embryonic stem cell
5 chr7:124892800-124898000 Enhancers iPS-15b Cell Line embryonic stem cell
6 chr7:124893200-124895400 Enhancers NHEK skin
7 chr7:124893600-124895000 Genic enhancers HUES64 Cell Line embryonic stem cell
8 chr7:124894000-124895000 Weak transcription Fetal Lung lung
9 chr7:124894200-124895200 Weak transcription Fetal Heart heart
10 chr7:124894200-124895600 Weak transcription ES-I3 Cell Line embryonic stem cell
11 chr7:124894400-124895000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr7:124894400-124895000 Enhancers HMEC breast
13 chr7:124894400-124895200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr7:124894800-124895400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr7:124894800-124896200 Genic enhancers HUES48 Cell Line embryonic stem cell
16 chr7:124894800-124896200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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