Variant report

Variant rs602738
Chromosome Location chr22:20970072-20970073
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:20964800-20974600 Weak transcription Esophagus oesophagus
2 chr22:20966400-20985600 Weak transcription Right Atrium heart
3 chr22:20967800-20973000 Weak transcription Primary Natural Killer cells fromperipheralblood blood
4 chr22:20967800-20973800 Weak transcription Spleen Spleen
5 chr22:20969600-20970400 Bivalent Enhancer K562 blood
6 chr22:20969800-20971000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr22:20970000-20970200 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
8 chr22:20970000-20970200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
9 chr22:20970000-20972800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr22:20970000-20975400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin

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