Variant report

Variant rs2279124
Chromosome Location chr11:67441553-67441554
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr11:67441000-67442200 Active TSS Esophagus oesophagus
8 chr11:67441000-67442200 Flanking Active TSS Placenta Placenta
9 chr11:67441200-67442200 Bivalent Enhancer Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr11:67441200-67443200 Enhancers Placenta Amnion Placenta Amnion
11 chr11:67441200-67443400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr11:67441400-67442200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr11:67441400-67442600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr11:67441400-67443000 Enhancers NHEK skin
15 chr11:67441400-67443400 Enhancers Stomach Mucosa stomach

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