| Tag | Content |
|---|
EnhancerAtlas ID | HS007-04352 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr13:20692390-20693250 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr13:20692999-20693020 | CCCCCTTCCCTCGCCTCCCCC | - | 7 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH13I020118 | chr13 | 20692140 | 20695980 |
| Enhancer Sequence | GGGGGGCCTT TCCGTTCCAA AGCAGATATT CTGGGCTATC TGACCTAACT CAGAGGAGGC 60
AGCCTCACCA TCCCACACCT GTCATCCTAG CGCTCAGGCC AGGCCCCTGG CGGGGAGCCT 120
CCAAGGGATG ACAGCGTGGC CCGCCCGAGG CCACAGGGAG GTGGGCGAGC TGTCACCTTC 180
GATGGGACAG CCCGGGCTGC GTCCTGAGCA CCCGGCCTGC CCAGGTGGCC TGGATCCTCG 240
GCGGGGTCCC CATCCCTCTG CTCCGAGTGC GCCGAGGGCC GCGTGGAGCC CGGAGCGCCA 300
GGGAGGGAGC CTGGAGGGCC GCCTGTCTTT TCGAGCTGCG CTTCCAGGGA CTTCGCGTTT 360
GTGCCTGGCG GGCTGCGGTT GGAAGAAAAG TGCCAACATG GCAGCTCCAG GGTCAGGCCC 420
CTTCTTCCAG GAGGCGTTTC TCAGCCACAC CAACGCGGCA CTTCTTTTCC CTTTTGGCAC 480
AGAAGTGAGG AAGAGCAGCT GAGCTGGTCT CGGTCTCCCA GCTCCTGCAG TCTGAGGACC 540
CCGGGATGCT CCAGCCAGGG CAGACCCGCG CGGGGGGTGC CCTTCCCCCA CCCCCTTCCC 600
TGCGGGATGC CCCCTTCCCT CGCCTCCCCC GCGGGGTGCC CCTTCGCTTC CCTCCCCACC 660
CCTTCCCCGC GGGGTGCCCC TCCTCCCGGT GTCGCCTCCT TTCAGGTGCC TGCCCCTCCC 720
CCATGTGTCT CCGCCCACGT CCGCCCCACC CCCACGCGTG TCGCCCCCGC CCCGTGTCCT 780
CCCCCGCCCC TGTGGAAGGG AGGCTGGGGC TCCCGGGACC AGCAGGGAAG CAGCTGGCAG 840
AGAACGTTGA GTGTTCTCTC 860
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