Variant report

Variant rs1039664
Chromosome Location chr7:65449716-65449717
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:65448200-65452800 Weak transcription K562 blood
2 chr7:65449000-65450200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr7:65449200-65449800 Enhancers A549 lung
4 chr7:65449200-65480400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr7:65449400-65449800 Enhancers Fetal Intestine Large intestine
6 chr7:65449600-65450800 Enhancers Hela-S3 cervix
7 chr7:65449600-65451800 Weak transcription HepG2 liver
8 chr7:65449600-65453200 Weak transcription Fetal Intestine Small intestine

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