Variant report

Variant rs13244579
Chromosome Location chr7:98798321-98798322
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:98792200-98803600 Weak transcription Stomach Mucosa stomach
2 chr7:98794800-98798400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr7:98797800-98800000 Enhancers Placenta Placenta
4 chr7:98798000-98798600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr7:98798000-98798800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr7:98798000-98799200 Enhancers NHEK skin
7 chr7:98798000-98799600 Enhancers HMEC breast
8 chr7:98798000-98800600 Weak transcription Primary T killer naive cells fromperipheralblood blood
9 chr7:98798200-98798600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr7:98798200-98798600 Weak transcription A549 lung
11 chr7:98798200-98799200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr7:98798200-98799200 Enhancers Osteobl bone
13 chr7:98798200-98799400 Enhancers Hela-S3 cervix

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