Variant report

Variant rs567508379
Chromosome Location chr4:9858825-9858826
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:9845000-9874800 Weak transcription NHEK skin
2 chr4:9848600-9861800 Weak transcription HMEC breast
3 chr4:9851200-9869800 Weak transcription Gastric stomach
4 chr4:9851400-9859000 Weak transcription HepG2 liver
5 chr4:9856800-9861200 Weak transcription Liver Liver
6 chr4:9857200-9864800 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr4:9858000-9862800 ZNF genes & repeats Breast Myoepithelial Primary Cells Breast
8 chr4:9858200-9859600 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr4:9858200-9861800 Weak transcription Fetal Intestine Large intestine
10 chr4:9858400-9867000 Strong transcription Monocytes-CD14+_RO01746 blood
11 chr4:9858800-9859400 Strong transcription Fetal Intestine Small intestine
12 chr4:9858800-9859600 ZNF genes & repeats Primary monocytes fromperipheralblood blood
13 chr4:9858800-9863200 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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