Variant report

Variant rs11914008
Chromosome Location chr22:23377865-23377866
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:23375200-23381200 Strong transcription Right Atrium heart
2 chr22:23375400-23381600 Enhancers Primary B cells from peripheral blood blood
3 chr22:23375800-23381400 Enhancers Primary B cells from cord blood blood
4 chr22:23376000-23378000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr22:23376200-23378800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr22:23376400-23378200 Weak transcription Fetal Brain Male brain
7 chr22:23376400-23378800 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr22:23376600-23381400 Enhancers Fetal Thymus thymus
9 chr22:23376800-23380000 Enhancers Dnd41 blood
10 chr22:23376800-23380400 Enhancers Thymus Thymus
11 chr22:23377000-23379200 Enhancers GM12878-XiMat blood
12 chr22:23377200-23378000 Flanking Bivalent TSS/Enh K562 blood
13 chr22:23377400-23378400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
14 chr22:23377800-23378800 Enhancers Primary Natural Killer cells fromperipheralblood blood
15 chr22:23377800-23379800 Bivalent Enhancer Primary T cells fromperipheralblood blood
16 chr22:23377800-23380000 Enhancers Primary T cells from cord blood blood
17 chr22:23377800-23380600 Enhancers Spleen Spleen

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