Variant report

Variant rs7774722
Chromosome Location chr6:141106027-141106028
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:141089600-141121800 Weak transcription Placenta Placenta
2 chr6:141103600-141106600 Weak transcription Fetal Intestine Large intestine
3 chr6:141105600-141106200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr6:141105600-141106400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr6:141105600-141106400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr6:141105600-141106400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr6:141105800-141106200 Enhancers Muscle Satellite Cultured Cells --
8 chr6:141105800-141106200 Enhancers HMEC breast
9 chr6:141105800-141106200 Enhancers NHEK skin
10 chr6:141105800-141106400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr6:141106000-141107200 Weak transcription Duodenum Mucosa Duodenum

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