Variant report

Variant rs73674657
Chromosome Location chr7:7189008-7189009
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr7:7188000-7189400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr7:7188200-7189200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr7:7188200-7189200 Enhancers HMEC breast
7 chr7:7188400-7189200 Flanking Active TSS HepG2 liver
8 chr7:7188400-7189400 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr7:7188400-7189600 Enhancers Placenta Placenta
10 chr7:7188400-7189600 Enhancers Stomach Mucosa stomach
11 chr7:7188600-7189200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr7:7188800-7196400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr7:7188800-7196400 Weak transcription Placenta Amnion Placenta Amnion
14 chr7:7189000-7189200 Enhancers K562 blood
15 chr7:7189000-7195800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr7:7189000-7196800 Weak transcription Duodenum Mucosa Duodenum

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