Variant report

Variant rs7762252
Chromosome Location chr6:132596481-132596482
allele C/T
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 chr6:132595800-132596600 Enhancers Fetal Muscle Trunk muscle
3 chr6:132595800-132596600 Enhancers Osteobl bone
4 chr6:132595800-132596800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr6:132595800-132596800 Enhancers Fetal Muscle Leg muscle
6 chr6:132595800-132597000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr6:132595800-132597000 Enhancers Gastric stomach
8 chr6:132596000-132596800 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr6:132596000-132596800 Flanking Active TSS Stomach Mucosa stomach
10 chr6:132596000-132597000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
11 chr6:132596200-132596600 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr6:132596200-132596600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr6:132596200-132596600 Active TSS Duodenum Mucosa Duodenum
14 chr6:132596200-132596600 Active TSS Fetal Intestine Large intestine
15 chr6:132596200-132596600 Flanking Active TSS Fetal Intestine Small intestine
16 chr6:132596200-132596600 Enhancers NHEK skin
17 chr6:132596400-132596800 Enhancers H9 Cell Line embryonic stem cell
18 chr6:132596400-132596800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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