Variant report

Variant rs4697911
Chromosome Location chr4:9902340-9902341
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 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 chr4:9894000-9917800 Weak transcription Lung lung
8 chr4:9894800-9903400 Weak transcription HepG2 liver
9 chr4:9895800-9906800 Weak transcription Right Atrium heart
10 chr4:9897000-9924600 Strong transcription Breast Myoepithelial Primary Cells Breast
11 chr4:9899400-9902400 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr4:9899800-9902600 Weak transcription Primary monocytes fromperipheralblood blood
13 chr4:9899800-9903600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr4:9900400-9911000 Weak transcription Aorta Aorta
15 chr4:9901000-9902800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
16 chr4:9901000-9910400 Weak transcription Duodenum Smooth Muscle Duodenum
17 chr4:9901200-9904200 Weak transcription HMEC breast
18 chr4:9902000-9903600 Weak transcription Monocytes-CD14+_RO01746 blood
19 chr4:9902000-9906800 Weak transcription Fetal Muscle Leg muscle
20 chr4:9902000-9907000 Weak transcription Fetal Stomach stomach
21 chr4:9902000-9909400 Weak transcription Adipose Nuclei Adipose
22 chr4:9902200-9902800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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