Variant report

Variant rs11250178
Chromosome Location chr8:11800234-11800235
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:11798800-11800600 Enhancers Left Ventricle heart
2 chr8:11798800-11800600 Enhancers Pancreas Pancrea
3 chr8:11798800-11800800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr8:11799200-11800800 Enhancers Fetal Adrenal Gland Adrenal Gland
5 chr8:11799400-11800400 Enhancers Fetal Intestine Large intestine
6 chr8:11799400-11800400 Flanking Bivalent TSS/Enh HepG2 liver
7 chr8:11799400-11800800 Enhancers Right Atrium heart
8 chr8:11799400-11800800 Enhancers Right Ventricle heart
9 chr8:11799600-11800400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr8:11799600-11800400 Enhancers Placenta Placenta
11 chr8:11799600-11800600 Enhancers Gastric stomach
12 chr8:11799800-11800400 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr8:11799800-11800400 Enhancers Ovary ovary
14 chr8:11799800-11800400 Flanking Active TSS K562 blood
15 chr8:11799800-11800600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr8:11800000-11800600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
17 chr8:11800000-11800800 Genic enhancers Foreskin Melanocyte Primary Cells skin01 Skin
18 chr8:11800000-11801000 Bivalent Enhancer Fetal Muscle Trunk muscle
19 chr8:11800200-11800600 Flanking Active TSS Fetal Heart heart
20 chr8:11800200-11800600 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
21 chr8:11800200-11801200 Weak transcription Fetal Intestine Small intestine
22 chr8:11800200-11804600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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