Variant report

Variant rs548847937
Chromosome Location chr4:9896465-9896466
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:9882600-9903600 Weak transcription Fetal Intestine Large intestine
2 chr4:9888800-9905800 Weak transcription Duodenum Mucosa Duodenum
3 chr4:9889000-9906200 Weak transcription Liver Liver
4 chr4:9890600-9905600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
5 chr4:9892200-9903600 Weak transcription Fetal Intestine Small intestine
6 chr4:9892800-9903600 Weak transcription NHEK skin
7 chr4:9893400-9897600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr4:9893400-9900200 Weak transcription HMEC breast
9 chr4:9893800-9899400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr4:9894000-9897000 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr4:9894000-9917800 Weak transcription Lung lung
12 chr4:9894200-9897600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr4:9894800-9903400 Weak transcription HepG2 liver
14 chr4:9895600-9896800 Strong transcription Monocytes-CD14+_RO01746 blood
15 chr4:9895800-9896800 Weak transcription Fetal Muscle Leg muscle
16 chr4:9895800-9906800 Weak transcription Right Atrium heart
17 chr4:9896200-9897400 Enhancers Primary monocytes fromperipheralblood blood
18 chr4:9896400-9896600 Enhancers iPS-20b Cell Line embryonic stem cell

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