Variant report

Variant rs35156535
Chromosome Location chr12:44642353-44642354
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:44612000-44655600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr12:44635800-44643400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr12:44641000-44643800 Weak transcription Duodenum Smooth Muscle Duodenum
4 chr12:44641600-44642800 ZNF genes & repeats Fetal Intestine Small intestine
5 chr12:44641600-44643800 Weak transcription Duodenum Mucosa Duodenum
6 chr12:44641800-44642400 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
7 chr12:44641800-44643000 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr12:44642000-44642600 ZNF genes & repeats Aorta Aorta
9 chr12:44642200-44642600 Strong transcription Breast Myoepithelial Primary Cells Breast
10 chr12:44642200-44642600 ZNF genes & repeats Gastric stomach

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