Variant report

Variant rs34225774
Chromosome Location chr8:11799618-11799619
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:11798600-11799800 Enhancers K562 blood
2 chr8:11798600-11800200 Enhancers Fetal Heart heart
3 chr8:11798800-11800200 Enhancers Fetal Intestine Small intestine
4 chr8:11798800-11800600 Enhancers Left Ventricle heart
5 chr8:11798800-11800600 Enhancers Pancreas Pancrea
6 chr8:11798800-11800800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr8:11799200-11800800 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr8:11799400-11800400 Enhancers Fetal Intestine Large intestine
9 chr8:11799400-11800400 Flanking Bivalent TSS/Enh HepG2 liver
10 chr8:11799400-11800800 Enhancers Right Atrium heart
11 chr8:11799400-11800800 Enhancers Right Ventricle heart
12 chr8:11799600-11800000 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
13 chr8:11799600-11800200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr8:11799600-11800200 Bivalent Enhancer Stomach Mucosa stomach
15 chr8:11799600-11800400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
16 chr8:11799600-11800400 Enhancers Placenta Placenta
17 chr8:11799600-11800600 Enhancers Gastric stomach

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