Variant report

Variant rs12281339
Chromosome Location chr11:59882012-59882013
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:59877000-59885000 Weak transcription Monocytes-CD14+_RO01746 blood
2 chr11:59877000-59885800 Weak transcription Primary monocytes fromperipheralblood blood
3 chr11:59878800-59882200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr11:59879200-59882400 Enhancers Fetal Intestine Small intestine
5 chr11:59879400-59897600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr11:59879800-59888200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr11:59880000-59883600 Weak transcription K562 blood
8 chr11:59880800-59882200 Enhancers Fetal Intestine Large intestine
9 chr11:59881000-59882200 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr11:59881000-59883800 Enhancers Ovary ovary
11 chr11:59881400-59882200 Enhancers H1 Cell Line embryonic stem cell
12 chr11:59881800-59882400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr11:59881800-59884000 Weak transcription iPS-18 Cell Line embryonic stem cell
14 chr11:59881800-59884200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr11:59881800-59888200 Weak transcription iPS-15b Cell Line embryonic stem cell

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