Variant report

Variant rs12281263
Chromosome Location chr11:15886388-15886389
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:15881200-15886600 Enhancers Fetal Heart heart
2 chr11:15883400-15887800 Weak transcription Right Atrium heart
3 chr11:15884600-15887600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
4 chr11:15885000-15886400 Enhancers HUES64 Cell Line embryonic stem cell
5 chr11:15885000-15887800 Enhancers Hela-S3 cervix
6 chr11:15885200-15886400 Enhancers Cortex derived primary cultured neurospheres brain
7 chr11:15885400-15886400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr11:15885400-15886600 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr11:15885600-15886400 Enhancers HUES6 Cell Line embryonic stem cell
10 chr11:15885600-15887000 Weak transcription Fetal Adrenal Gland Adrenal Gland
11 chr11:15885600-15887400 Enhancers Placenta Placenta
12 chr11:15885600-15888000 Enhancers Esophagus oesophagus
13 chr11:15885800-15886400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr11:15885800-15886600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
15 chr11:15886000-15886400 Weak transcription H9 Cell Line embryonic stem cell
16 chr11:15886000-15886800 Enhancers NHEK skin
17 chr11:15886000-15888000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr11:15886000-15888400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
19 chr11:15886200-15886400 Flanking Active TSS iPS-20b Cell Line embryonic stem cell
20 chr11:15886200-15886800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell

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