Variant report

Variant rs11033508
Chromosome Location chr11:36262540-36262541
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:36236800-36273200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr11:36249000-36262800 Weak transcription Spleen Spleen
3 chr11:36250800-36270600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr11:36252200-36270600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr11:36252200-36277800 Weak transcription Esophagus oesophagus
6 chr11:36253800-36270400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr11:36254400-36265400 Weak transcription Fetal Muscle Leg muscle
8 chr11:36255000-36264600 Weak transcription Fetal Stomach stomach
9 chr11:36255000-36273000 Weak transcription Brain Germinal Matrix brain
10 chr11:36257600-36270400 Weak transcription Muscle Satellite Cultured Cells --
11 chr11:36257800-36271600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr11:36260800-36263000 Enhancers Fetal Brain Female brain
13 chr11:36260800-36263600 Enhancers Fetal Brain Male brain
14 chr11:36261200-36263000 Enhancers Cortex derived primary cultured neurospheres brain
15 chr11:36262000-36263000 Enhancers HSMMtube muscle
16 chr11:36262200-36262600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
17 chr11:36262400-36271600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain

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