Variant report

Variant rs13080973
Chromosome Location chr3:138596050-138596051
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:138594600-138596400 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
2 chr3:138595000-138596200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr3:138595200-138598200 Weak transcription Stomach Mucosa stomach
4 chr3:138595200-138598400 Weak transcription Duodenum Mucosa Duodenum
5 chr3:138595200-138598400 Weak transcription HepG2 liver
6 chr3:138595400-138596600 Enhancers Primary neutrophils fromperipheralblood blood
7 chr3:138595400-138598200 Weak transcription Fetal Intestine Small intestine
8 chr3:138595400-138600200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr3:138595400-138604600 Weak transcription Primary monocytes fromperipheralblood blood
10 chr3:138595800-138596600 Flanking Active TSS K562 blood
11 chr3:138595800-138596800 Enhancers Breast Myoepithelial Primary Cells Breast
12 chr3:138595800-138597200 Enhancers NHEK skin
13 chr3:138596000-138596200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr3:138596000-138596400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr3:138596000-138596400 Flanking Active TSS HMEC breast
16 chr3:138596000-138596800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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