Variant report

Variant rs11855692
Chromosome Location chr15:52749729-52749730
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:52732600-52750600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr15:52734600-52753200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr15:52739000-52751800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr15:52739000-52753600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr15:52740400-52756200 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
6 chr15:52740600-52753200 Weak transcription Monocytes-CD14+_RO01746 blood
7 chr15:52742000-52755800 Weak transcription Primary T helper naive cells fromperipheralblood blood
8 chr15:52742200-52751600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr15:52742200-52753000 Weak transcription NHEK skin
10 chr15:52743800-52758200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr15:52747400-52753200 Weak transcription Muscle Satellite Cultured Cells --
12 chr15:52748200-52755600 Weak transcription Primary B cells from cord blood blood
13 chr15:52748400-52752800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
14 chr15:52749600-52752200 Genic enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr15:52749600-52752800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
16 chr15:52749600-52756600 Weak transcription Primary mononuclear cells fromperipheralblood Blood

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