Variant report

Variant rs7667325
Chromosome Location chr4:175318697-175318698
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:175316000-175320000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr4:175316000-175320200 Weak transcription NH-A brain
3 chr4:175316200-175319800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr4:175316200-175319800 Weak transcription NHLF lung
5 chr4:175317200-175319600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr4:175317400-175319200 Enhancers Rectal Mucosa Donor 31 rectum
7 chr4:175317600-175319600 Weak transcription Muscle Satellite Cultured Cells --
8 chr4:175317800-175319600 Weak transcription NHDF-Ad bronchial
9 chr4:175318200-175319200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr4:175318400-175319200 Enhancers Fetal Intestine Large intestine
11 chr4:175318400-175320800 Enhancers A549 lung
12 chr4:175318600-175319600 Enhancers Sigmoid Colon Sigmoid Colon
13 chr4:175318600-175322800 Weak transcription ES-WA7 Cell Line embryonic stem cell

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