Variant report

Variant rs147134430
Chromosome Location chr11:75883772-75883773
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:75876600-75884400 Weak transcription Esophagus oesophagus
2 chr11:75877600-75887200 Weak transcription Skeletal Muscle Male skeletal muscle
3 chr11:75879800-75886600 Weak transcription Fetal Muscle Leg muscle
4 chr11:75881000-75887200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr11:75882600-75883800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
6 chr11:75883000-75883800 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
7 chr11:75883400-75884000 Bivalent Enhancer Fetal Stomach stomach
8 chr11:75883600-75884200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
9 chr11:75883600-75897000 Weak transcription Fetal Intestine Small intestine

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