Variant report

Variant rs568031783
Chromosome Location chr19:41451903-41451904
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:41444800-41455800 Weak transcription Fetal Intestine Large intestine
2 chr19:41451400-41452200 Flanking Active TSS K562 blood
3 chr19:41451800-41452200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr19:41451800-41455200 Weak transcription Liver Liver
5 chr19:41451800-41456200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr19:41451800-41456200 Weak transcription Fetal Intestine Small intestine

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