Variant report

Variant rs7899763
Chromosome Location chr10:44776562-44776563
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:44774000-44777000 Enhancers NHLF lung
2 chr10:44774000-44780000 Enhancers Fetal Brain Male brain
3 chr10:44774200-44777400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr10:44774600-44776600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr10:44774600-44776800 Enhancers Colon Smooth Muscle Colon
6 chr10:44774600-44777000 Enhancers Fetal Brain Female brain
7 chr10:44775000-44777000 Enhancers Brain Germinal Matrix brain
8 chr10:44775200-44779800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr10:44775600-44777000 Enhancers Aorta Aorta
10 chr10:44775800-44776600 Flanking Active TSS NHDF-Ad bronchial
11 chr10:44775800-44777600 Enhancers Fetal Muscle Leg muscle
12 chr10:44776200-44776800 Enhancers Fetal Stomach stomach
13 chr10:44776200-44777000 Enhancers Skeletal Muscle Female skeletal muscle
14 chr10:44776400-44776600 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr10:44776400-44776600 Enhancers Fetal Muscle Trunk muscle
16 chr10:44776400-44777000 Flanking Active TSS Adipose Nuclei Adipose
17 chr10:44776400-44777000 Enhancers HepG2 liver
18 chr10:44776400-44777400 Enhancers Right Atrium heart

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