Variant report

Variant rs56391020
Chromosome Location chr12:9607624-9607625
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:9602200-9608000 Weak transcription HUVEC blood vessel
2 chr12:9606600-9607800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
3 chr12:9606600-9607800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr12:9606800-9608800 Enhancers Fetal Heart heart
5 chr12:9607000-9608200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr12:9607200-9608200 Weak transcription NHEK skin
7 chr12:9607200-9608400 Weak transcription K562 blood
8 chr12:9607200-9623000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
9 chr12:9607400-9608200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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