Variant report

Variant rs9504324
Chromosome Location chr6:5090652-5090653
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:28 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:5087400-5090800 Enhancers HepG2 liver
2 chr6:5089600-5091000 Enhancers Monocytes-CD14+_RO01746 blood
3 chr6:5089800-5091000 Enhancers Primary monocytes fromperipheralblood blood
4 chr6:5090000-5090800 Enhancers Fetal Intestine Small intestine
5 chr6:5090000-5092600 Enhancers Primary B cells from peripheral blood blood
6 chr6:5090200-5090800 Bivalent Enhancer Primary T cells from cord blood blood
7 chr6:5090200-5091000 Enhancers Right Atrium heart
8 chr6:5090200-5091200 Enhancers Left Ventricle heart
9 chr6:5090200-5091400 Enhancers Fetal Heart heart
10 chr6:5090400-5090800 Bivalent Enhancer Placenta Placenta
11 chr6:5090400-5090800 Enhancers Rectal Mucosa Donor 31 rectum
12 chr6:5090400-5090800 Bivalent Enhancer HUVEC blood vessel
13 chr6:5090400-5091000 Enhancers Right Ventricle heart
14 chr6:5090400-5091000 Enhancers Spleen Spleen
15 chr6:5090400-5091400 Enhancers Fetal Adrenal Gland Adrenal Gland
16 chr6:5090400-5091400 Bivalent Enhancer Fetal Thymus thymus
17 chr6:5090400-5091600 Enhancers Fetal Muscle Leg muscle
18 chr6:5090400-5092400 Flanking Active TSS GM12878-XiMat blood
19 chr6:5090600-5090800 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
20 chr6:5090600-5091000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
21 chr6:5090600-5091000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
22 chr6:5090600-5091000 Strong transcription Aorta Aorta
23 chr6:5090600-5091000 Bivalent Enhancer Fetal Muscle Trunk muscle
24 chr6:5090600-5091000 Bivalent Enhancer Lung lung
25 chr6:5090600-5091000 Enhancers Pancreas Pancrea
26 chr6:5090600-5091600 Enhancers Adipose Nuclei Adipose
27 chr6:5090600-5093600 Weak transcription Brain Anterior Caudate brain
28 chr6:5090600-5095600 Weak transcription Sigmoid Colon Sigmoid Colon

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