Variant report

Variant rs11975595
Chromosome Location chr7:3448535-3448536
allele C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:3443800-3450200 Enhancers Pancreatic Islets Pancreatic Islet
2 chr7:3444400-3451800 Weak transcription Fetal Brain Female brain
3 chr7:3444800-3454800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr7:3445000-3448800 Weak transcription NHEK skin
5 chr7:3446200-3449000 Weak transcription Aorta Aorta
6 chr7:3447000-3457000 Weak transcription Fetal Kidney kidney
7 chr7:3447600-3448600 Weak transcription Left Ventricle heart
8 chr7:3447600-3449000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr7:3447600-3450400 Weak transcription Pancreas Pancrea
10 chr7:3448000-3449000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr7:3448000-3449000 Enhancers Fetal Heart heart
12 chr7:3448400-3448800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
13 chr7:3448400-3449000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr7:3448400-3449000 Enhancers Brain Germinal Matrix brain
15 chr7:3448400-3449200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr7:3448400-3449400 Enhancers Fetal Brain Male brain
17 chr7:3448400-3449400 Enhancers Fetal Lung lung
18 chr7:3448400-3449400 Enhancers HSMMtube muscle
19 chr7:3448400-3449600 Enhancers Primary T cells from cord blood blood

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