Variant report

Variant rs61839802
Chromosome Location chr1:246619589-246619590
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246602000-246622800 Weak transcription Primary hematopoietic stem cells short term culture blood
2 chr1:246609600-246621200 Weak transcription Fetal Heart heart
3 chr1:246611200-246625000 Weak transcription Osteobl bone
4 chr1:246614000-246625600 Weak transcription Fetal Kidney kidney
5 chr1:246617600-246619600 Weak transcription Psoas Muscle Psoas
6 chr1:246618000-246623400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr1:246619000-246639600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr1:246619400-246619800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:246619400-246619800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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