Variant report

Variant rs541413624
Chromosome Location chr11:71515455-71515456
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:71499400-71515600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr11:71500400-71515600 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr11:71506000-71515600 Weak transcription H9 Cell Line embryonic stem cell
4 chr11:71506400-71515600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
5 chr11:71506600-71515600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr11:71508200-71524400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr11:71508800-71524400 Weak transcription Fetal Intestine Small intestine
8 chr11:71511600-71523600 Weak transcription Brain Inferior Temporal Lobe brain
9 chr11:71511600-71524400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
10 chr11:71511600-71524400 Weak transcription Brain Angular Gyrus brain
11 chr11:71513600-71515600 Weak transcription Fetal Muscle Leg muscle
12 chr11:71515200-71515800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr11:71515200-71515800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr11:71515200-71515800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr11:71515200-71515800 Enhancers Fetal Intestine Large intestine
16 chr11:71515200-71515800 Enhancers Lung lung

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