Variant report

Variant rs142472391
Chromosome Location chr2:40158600-40158601
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:40141600-40164800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr2:40147000-40167400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr2:40152000-40158800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr2:40156400-40160200 Weak transcription Fetal Stomach stomach
5 chr2:40156800-40158600 Weak transcription HSMM muscle
6 chr2:40156800-40158800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr2:40157000-40159200 Genic enhancers Dnd41 blood
8 chr2:40157600-40158600 Enhancers Fetal Thymus thymus
9 chr2:40158600-40158800 Genic enhancers Fetal Thymus thymus
10 chr2:40158600-40159200 ZNF genes & repeats HSMM muscle

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