Variant report

Variant rs1106059
Chromosome Location chr4:9861512-9861513
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr4:9857200-9864800 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr4:9858000-9862800 ZNF genes & repeats Breast Myoepithelial Primary Cells Breast
6 chr4:9858200-9861800 Weak transcription Fetal Intestine Large intestine
7 chr4:9858400-9867000 Strong transcription Monocytes-CD14+_RO01746 blood
8 chr4:9858800-9863200 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr4:9859400-9861600 Weak transcription HepG2 liver
10 chr4:9859800-9862600 Weak transcription Small Intestine intestine
11 chr4:9860200-9861800 Weak transcription Duodenum Mucosa Duodenum
12 chr4:9861000-9864800 Weak transcription Primary mononuclear cells fromperipheralblood Blood
13 chr4:9861200-9863400 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr4:9861200-9863600 Strong transcription Liver Liver
15 chr4:9861400-9862600 Strong transcription Fetal Intestine Small intestine
16 chr4:9861400-9864400 Strong transcription Primary monocytes fromperipheralblood blood

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