Variant report

Variant rs12540384
Chromosome Location chr7:102502063-102502064
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:102470000-102516400 Weak transcription Pancreas Pancrea
2 chr7:102500400-102503600 Weak transcription Placenta Amnion Placenta Amnion
3 chr7:102500600-102502600 Weak transcription H9 Cell Line embryonic stem cell
4 chr7:102500600-102513800 Weak transcription Aorta Aorta
5 chr7:102500600-102514200 Weak transcription Duodenum Smooth Muscle Duodenum
6 chr7:102500600-102518400 Weak transcription Left Ventricle heart
7 chr7:102501000-102504600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr7:102501000-102505800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr7:102501000-102511200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
10 chr7:102501000-102512200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
11 chr7:102501200-102503000 Weak transcription A549 lung
12 chr7:102501200-102504400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
13 chr7:102501200-102504600 Weak transcription K562 blood
14 chr7:102501200-102506800 Weak transcription Fetal Kidney kidney
15 chr7:102501200-102515800 Weak transcription Gastric stomach
16 chr7:102501200-102530800 Weak transcription Ovary ovary
17 chr7:102501400-102503200 Weak transcription Fetal Lung lung
18 chr7:102501400-102504200 Weak transcription Muscle Satellite Cultured Cells --
19 chr7:102501400-102504600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
20 chr7:102501600-102503000 Enhancers Fetal Stomach stomach
21 chr7:102501600-102504600 Weak transcription HUVEC blood vessel
22 chr7:102502000-102508800 Weak transcription HepG2 liver

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