Variant report

Variant rs1235044
Chromosome Location chr11:121798489-121798490
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:121793000-121799000 Weak transcription Fetal Kidney kidney
2 chr11:121797400-121799600 Enhancers HepG2 liver
3 chr11:121797400-121800000 Enhancers Fetal Brain Male brain
4 chr11:121797800-121799000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
5 chr11:121797800-121799400 Enhancers Brain Germinal Matrix brain
6 chr11:121797800-121803800 Enhancers Liver Liver
7 chr11:121798000-121798600 Enhancers HUES6 Cell Line embryonic stem cell
8 chr11:121798200-121799400 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr11:121798200-121799400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
10 chr11:121798200-121799600 Enhancers HUES48 Cell Line embryonic stem cell
11 chr11:121798200-121799800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
12 chr11:121798200-121800000 Enhancers Fetal Stomach stomach
13 chr11:121798200-121800200 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
14 chr11:121798400-121799400 Weak transcription H9 Cell Line embryonic stem cell
15 chr11:121798400-121799400 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
16 chr11:121798400-121799400 Enhancers Fetal Brain Female brain

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