Variant report

Variant rs57040652
Chromosome Location chr5:80578610-80578611
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:80565200-80580400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr5:80566200-80587800 Weak transcription Ovary ovary
3 chr5:80566400-80581400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr5:80566400-80587600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr5:80566800-80587600 Weak transcription Right Ventricle heart
6 chr5:80568000-80585600 Weak transcription Skeletal Muscle Male skeletal muscle
7 chr5:80570400-80587200 Weak transcription Primary B cells from cord blood blood
8 chr5:80571600-80583000 Weak transcription Primary T helper cells fromperipheralblood blood
9 chr5:80571800-80579600 Weak transcription Fetal Heart heart
10 chr5:80572000-80595200 Weak transcription Rectal Mucosa Donor 29 rectum
11 chr5:80572400-80578800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr5:80573800-80587400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
13 chr5:80574600-80585600 Weak transcription Dnd41 blood
14 chr5:80577200-80586200 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
15 chr5:80578000-80579800 Weak transcription Breast Myoepithelial Primary Cells Breast
16 chr5:80578000-80586800 Weak transcription Skeletal Muscle Female skeletal muscle
17 chr5:80578200-80582400 Weak transcription ES-WA7 Cell Line embryonic stem cell
18 chr5:80578200-80585200 Weak transcription Fetal Intestine Large intestine
19 chr5:80578200-80585600 Weak transcription Left Ventricle heart
20 chr5:80578600-80579000 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin

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