Variant report

Variant rs9639559
Chromosome Location chr7:27605495-27605496
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:27559400-27627800 Weak transcription Psoas Muscle Psoas
2 chr7:27580600-27615000 Weak transcription Aorta Aorta
3 chr7:27581400-27617400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr7:27582400-27650800 Weak transcription Left Ventricle heart
5 chr7:27582800-27615000 Weak transcription Placenta Placenta
6 chr7:27582800-27615200 Weak transcription Ovary ovary
7 chr7:27600600-27645600 Weak transcription Colon Smooth Muscle Colon
8 chr7:27601200-27609600 Weak transcription Osteobl bone
9 chr7:27603000-27626400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
10 chr7:27603200-27615400 Weak transcription Adipose Nuclei Adipose
11 chr7:27603200-27631800 Weak transcription Primary T cells from cord blood blood
12 chr7:27603400-27606600 Weak transcription HSMM muscle
13 chr7:27603400-27608600 Weak transcription NHDF-Ad bronchial
14 chr7:27603400-27609000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr7:27603600-27626400 Weak transcription Duodenum Smooth Muscle Duodenum
16 chr7:27604600-27605600 ZNF genes & repeats Liver Liver
17 chr7:27604800-27605800 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr7:27605000-27606600 Weak transcription Fetal Lung lung
19 chr7:27605000-27614800 Weak transcription Fetal Kidney kidney
20 chr7:27605200-27615400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
21 chr7:27605200-27617200 Weak transcription Fetal Intestine Small intestine
22 chr7:27605200-27624400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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