Variant report

Variant rs66891779
Chromosome Location chr4:22362578-22362579
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:22329000-22389400 Weak transcription Pancreas Pancrea
2 chr4:22336600-22385400 Weak transcription Fetal Intestine Large intestine
3 chr4:22354000-22378200 Weak transcription Aorta Aorta
4 chr4:22356200-22364000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr4:22359000-22365000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr4:22362000-22363000 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr4:22362200-22362800 Enhancers iPS-15b Cell Line embryonic stem cell
8 chr4:22362200-22362800 Enhancers iPS-20b Cell Line embryonic stem cell
9 chr4:22362400-22362600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
10 chr4:22362400-22362800 Enhancers H9 Cell Line embryonic stem cell
11 chr4:22362400-22362800 Enhancers HUES6 Cell Line embryonic stem cell
12 chr4:22362400-22366400 Weak transcription Ovary ovary

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