Variant report

Variant rs12081562
Chromosome Location chr1:169176266-169176267
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:169130400-169195200 Weak transcription Pancreas Pancrea
2 chr1:169163600-169184000 Weak transcription Ovary ovary
3 chr1:169167200-169176400 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr1:169167800-169186800 Weak transcription Primary T cells from cord blood blood
5 chr1:169168000-169183800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr1:169171600-169184000 Weak transcription Fetal Intestine Small intestine
7 chr1:169172000-169176600 Weak transcription Colon Smooth Muscle Colon
8 chr1:169172400-169183800 Weak transcription Brain Germinal Matrix brain
9 chr1:169172400-169207600 Weak transcription Esophagus oesophagus
10 chr1:169172600-169227000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:169173200-169202000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr1:169173600-169183800 Weak transcription Primary hematopoietic stem cells short term culture blood

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