Variant report

Variant rs4121361
Chromosome Location chr11:102628585-102628586
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:102620600-102628600 Weak transcription HMEC breast
2 chr11:102620600-102628800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr11:102622800-102632400 Weak transcription ES-I3 Cell Line embryonic stem cell
4 chr11:102623000-102632600 Weak transcription H9 Cell Line embryonic stem cell
5 chr11:102624200-102632400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr11:102624400-102628800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr11:102624600-102628600 Weak transcription NHEK skin
8 chr11:102624600-102632400 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr11:102624800-102628800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr11:102624800-102633600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr11:102628200-102629200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr11:102628200-102629200 Enhancers Primary hematopoietic stem cells blood
13 chr11:102628200-102629200 Enhancers Primary hematopoietic stem cells short term culture blood
14 chr11:102628200-102629400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr11:102628200-102629600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr11:102628200-102631400 Enhancers Primary monocytes fromperipheralblood blood
17 chr11:102628400-102628600 Enhancers Monocytes-CD14+_RO01746 blood

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