Variant report

Variant rs11207257
Chromosome Location chr1:59016136-59016137
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:59012600-59016200 Weak transcription Primary mononuclear cells fromperipheralblood Blood
2 chr1:59012800-59016600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr1:59012800-59017400 Weak transcription Pancreas Pancrea
4 chr1:59012800-59017600 Weak transcription Aorta Aorta
5 chr1:59013000-59016600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr1:59013000-59016600 Weak transcription Brain Hippocampus Middle brain
7 chr1:59013000-59016600 Weak transcription Brain Inferior Temporal Lobe brain
8 chr1:59013200-59017000 Weak transcription Fetal Brain Male brain
9 chr1:59014600-59016400 Enhancers Fetal Intestine Small intestine
10 chr1:59014600-59018000 Enhancers Fetal Lung lung
11 chr1:59014800-59017400 Weak transcription Ovary ovary
12 chr1:59015200-59016200 Enhancers Fetal Intestine Large intestine
13 chr1:59015200-59016400 Enhancers Fetal Kidney kidney
14 chr1:59015800-59016800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr1:59015800-59017800 Enhancers K562 blood
16 chr1:59016000-59016400 Weak transcription Placenta Placenta

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