Variant report

Variant rs4646819
Chromosome Location chr11:67441052-67441053
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:67434000-67442400 Weak transcription Fetal Intestine Small intestine
2 chr11:67437200-67441600 Weak transcription Gastric stomach
3 chr11:67438000-67442000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr11:67439000-67442000 Weak transcription Dnd41 blood
5 chr11:67440800-67441800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr11:67440800-67443200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr11:67441000-67441200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
8 chr11:67441000-67441200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr11:67441000-67441200 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
10 chr11:67441000-67441400 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr11:67441000-67442200 Active TSS Esophagus oesophagus
12 chr11:67441000-67442200 Flanking Active TSS Placenta Placenta

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