Variant report

Variant rs73674662
Chromosome Location chr7:7190527-7190528
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:7187600-7190800 Enhancers Fetal Intestine Large intestine
2 chr7:7187800-7190800 Enhancers Fetal Intestine Small intestine
3 chr7:7187800-7191000 Weak transcription Primary T helper cells PMA-I stimulated --
4 chr7:7188800-7196400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr7:7188800-7196400 Weak transcription Placenta Amnion Placenta Amnion
6 chr7:7189000-7195800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr7:7189000-7196800 Weak transcription Duodenum Mucosa Duodenum
8 chr7:7189200-7199600 Weak transcription K562 blood
9 chr7:7189400-7191200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr7:7189600-7191800 Weak transcription Placenta Placenta
11 chr7:7189600-7196400 Weak transcription Stomach Mucosa stomach
12 chr7:7190000-7191800 Enhancers Primary T helper memory cells from peripheral blood 1 blood
13 chr7:7190200-7191400 Enhancers HepG2 liver

Quick Search:


  
Input of quick search could be:

what's new

Quick links