Variant report

Variant rs76769213
Chromosome Location chr11:75881094-75881095
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:75873600-75882200 Weak transcription Right Atrium heart
2 chr11:75873800-75881600 Weak transcription Pancreas Pancrea
3 chr11:75876600-75884400 Weak transcription Esophagus oesophagus
4 chr11:75877600-75887200 Weak transcription Skeletal Muscle Male skeletal muscle
5 chr11:75878400-75882600 Bivalent Enhancer Fetal Muscle Trunk muscle
6 chr11:75879600-75881200 Enhancers GM12878-XiMat blood
7 chr11:75879800-75886600 Weak transcription Fetal Muscle Leg muscle
8 chr11:75880600-75881200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr11:75880600-75881200 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr11:75880600-75881800 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
11 chr11:75881000-75881200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
12 chr11:75881000-75881200 Bivalent/Poised TSS HepG2 liver
13 chr11:75881000-75882600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
14 chr11:75881000-75887200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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