Variant report

Variant rs67671118
Chromosome Location chr4:175592513-175592514
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:175585000-175593200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr4:175590200-175595000 Weak transcription Fetal Intestine Small intestine
3 chr4:175590600-175593200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr4:175591000-175593000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr4:175591000-175593200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr4:175591000-175593400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr4:175591000-175593600 Weak transcription HMEC breast
8 chr4:175591000-175595400 Weak transcription Hela-S3 cervix
9 chr4:175591200-175593000 Weak transcription K562 blood
10 chr4:175591800-175593200 Weak transcription A549 lung
11 chr4:175591800-175595200 Weak transcription Fetal Intestine Large intestine

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