Variant report

Variant rs490749
Chromosome Location chr22:20972176-20972177
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 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 chr22:20970000-20972800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr22:20970000-20975400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr22:20970200-20975400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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