Variant report

Variant rs6967389
Chromosome Location chr7:102490701-102490702
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:102470000-102516400 Weak transcription Pancreas Pancrea
2 chr7:102470800-102493200 Weak transcription Primary T cells from cord blood blood
3 chr7:102471800-102500000 Weak transcription Left Ventricle heart
4 chr7:102477800-102500800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr7:102478200-102500000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr7:102478200-102500000 Weak transcription Ovary ovary
7 chr7:102478800-102492600 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr7:102482800-102499600 Weak transcription Fetal Lung lung
9 chr7:102482800-102500200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
10 chr7:102483000-102491200 Weak transcription Fetal Stomach stomach
11 chr7:102483400-102499600 Weak transcription K562 blood
12 chr7:102489200-102491600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr7:102489200-102492400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr7:102490000-102499600 Weak transcription Aorta Aorta
15 chr7:102490400-102491200 Weak transcription Gastric stomach
16 chr7:102490400-102500000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr7:102490400-102500000 Weak transcription NHDF-Ad bronchial

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