Variant report

Variant rs201449963
Chromosome Location chr12:9606644-9606645
allele -/GAA
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:9601800-9606800 Weak transcription Fetal Adrenal Gland Adrenal Gland
2 chr12:9602000-9606800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr12:9602200-9606800 Weak transcription Fetal Heart heart
4 chr12:9602200-9608000 Weak transcription HUVEC blood vessel
5 chr12:9606200-9607400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr12:9606400-9607200 Enhancers NHEK skin
7 chr12:9606400-9607600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr12:9606600-9607000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr12:9606600-9607200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
10 chr12:9606600-9607200 Enhancers K562 blood
11 chr12:9606600-9607800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr12:9606600-9607800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --

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