Variant report

Variant rs144778219
Chromosome Location chr12:9606863-9606864
allele -/GG
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:9602200-9608000 Weak transcription HUVEC blood vessel
2 chr12:9606200-9607400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr12:9606400-9607200 Enhancers NHEK skin
4 chr12:9606400-9607600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr12:9606600-9607000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr12:9606600-9607200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
7 chr12:9606600-9607200 Enhancers K562 blood
8 chr12:9606600-9607800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr12:9606600-9607800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr12:9606800-9607200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr12:9606800-9607200 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr12:9606800-9608800 Enhancers Fetal Heart heart

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