Variant report

Variant rs535413
Chromosome Location chr11:59898111-59898112
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:59892600-59899200 Weak transcription Fetal Intestine Large intestine
2 chr11:59893800-59899400 Weak transcription Rectal Mucosa Donor 31 rectum
3 chr11:59895000-59899200 Weak transcription Ovary ovary
4 chr11:59895400-59907400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr11:59895800-59899200 Weak transcription Fetal Intestine Small intestine
6 chr11:59897400-59898200 Enhancers Primary B cells from peripheral blood blood
7 chr11:59897400-59898400 Enhancers K562 blood
8 chr11:59897600-59898400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr11:59897600-59898400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
10 chr11:59897600-59898400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
11 chr11:59898000-59898200 Enhancers HUES48 Cell Line embryonic stem cell
12 chr11:59898000-59898200 Enhancers HUES6 Cell Line embryonic stem cell
13 chr11:59898000-59898200 Enhancers iPS-18 Cell Line embryonic stem cell
14 chr11:59898000-59898600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --

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