Variant report

Variant rs117311876
Chromosome Location chr11:75880444-75880445
allele A/G
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 chr11:75876600-75880600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr11:75876600-75884400 Weak transcription Esophagus oesophagus
5 chr11:75877600-75880600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr11:75877600-75887200 Weak transcription Skeletal Muscle Male skeletal muscle
7 chr11:75878400-75881000 Enhancers Placenta Placenta
8 chr11:75878400-75882600 Bivalent Enhancer Fetal Muscle Trunk muscle
9 chr11:75879600-75881200 Enhancers GM12878-XiMat blood
10 chr11:75879800-75886600 Weak transcription Fetal Muscle Leg muscle
11 chr11:75880000-75880600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
12 chr11:75880200-75881000 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin02 Skin
13 chr11:75880400-75881000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
14 chr11:75880400-75881000 Flanking Bivalent TSS/Enh HepG2 liver

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