Variant report

Variant rs9483425
Chromosome Location chr6:132596741-132596742
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:132594200-132599200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr6:132595800-132596800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr6:132595800-132596800 Enhancers Fetal Muscle Leg muscle
4 chr6:132595800-132597000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr6:132595800-132597000 Enhancers Gastric stomach
6 chr6:132596000-132596800 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr6:132596000-132596800 Flanking Active TSS Stomach Mucosa stomach
8 chr6:132596000-132597000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
9 chr6:132596400-132596800 Enhancers H9 Cell Line embryonic stem cell
10 chr6:132596400-132596800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr6:132596600-132596800 Flanking Active TSS Duodenum Mucosa Duodenum
12 chr6:132596600-132597000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
13 chr6:132596600-132597000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr6:132596600-132597000 Enhancers Fetal Intestine Large intestine
15 chr6:132596600-132597000 Active TSS K562 blood
16 chr6:132596600-132597400 Enhancers Fetal Intestine Small intestine
17 chr6:132596600-132600800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr6:132596600-132600800 Weak transcription Fetal Muscle Trunk muscle

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