| Tag | Content |
|---|
EnhancerAtlas ID | HS076-29877 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr19:45768170-45769480 |
Target genes | | Number: 45 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr19:45768261-45768272 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr19:45768262-45768272 | GGGGCGGGGC | - | 6.02 | | SP1 | MA0079.4 | chr19:45768260-45768275 | TGGGGGCGGGGCTTA | - | 6.95 | | SP2 | MA0516.2 | chr19:45768259-45768276 | CTGGGGGCGGGGCTTAA | - | 7.07 | | SP4 | MA0685.1 | chr19:45768258-45768275 | CCTGGGGGCGGGGCTTA | - | 6.35 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 45769155 | 45769211 | | chr19 | 45769267 | 45769429 |
|
Enhancer Sequence | TGGGGCAGGG CTGAGGGTGG GGCTGACTGG GTGCCTGGGT CCCTGGGAGG GCGTCTGAGA 60
GCTGGGCATG GTCTGGGCTG TCCAGCGACC TGGGGGCGGG GCTTAAGTCT GGGCAGGGGT 120
GAAGGTGCAG AGCTGGGTGT GCTGGGCATA TAGTTGCCCA GATGTGAGGG CATCCGGATG 180
TAGGTTTGCA GGTGCCCCGT TGGGTGGGTG AGAGGATGTT TGGGCATGAA GGCGCCCCGG 240
TGGGCAGGTG TTGCATGTGT AGGGCATGTG GGTGTGCCCA GCGCGTAGGT GTGTGGGTGA 300
TGGGGGCACG AAGGTGCCAG GGTGCCAGGT GTGAGTGTGC CGGAGTGTGA TTCAAAAGAT 360
GTGTGGGCAG TAGCTATGTG GGTGCCCAGG TATGTAGGTA TGTAGGTGTG TGGGGAAGAG 420
AGTGTAGGGC ACCCCAGGTA GATGGGCAAG AGAGGGCTGA GGGGTGGTTG TGTAAGCTTG 480
TAGGTACTAG GGCATGCCGG TATGTGGGTG CCCGGGTGTG CGAGTGCCCA GATGTATGGG 540
TTTCCAGGTG TGTGGTAGTG AGGACACCCA GGTGTGTAAG AGTGTGGGGG GGGCCAGGTG 600
TGGAGTAAGA GGACGTGCAG GTGTGAGGGT GCCCAGGTAT GTGGGATAAG AAGAAGTGCA 660
GGTATAAGGG TGCCCAGGTG TGGGGTAAGA ATATGTGCAG GTGTGAGGGT GCCCAGGTGT 720
GGGGTAAGAG GAGATGCAGG TATGAAGGTG CCCAGGTGTG GGGTAAGAGG AGTTGTGGGT 780
GTGAGGGTGC TGGGGCATGA GGGGTAAGAA GATGTGCGTG TGTGAGGGTG CCAGGTGTGT 840
GGGGTAAGAG GAGATGCAGG TGTGAGGGTG CCGGGGCATG TGGGGTAAGC AGATGTGCAG 900
GTGTGAGGGT GCCGGGCATG TCGGCTAGGA AGATGTGCAG GTGTGAGGGT GTTTCTGCCT 960
TGACGCTGCT GTCCTGAACT CAAGGGCCAT AAGCCCTGGT GAGTTGGGGC GGCCTGTCTA 1020
TCTACAGGTA TGGGATATCC CCATGGGAGT TTCCAGATGT GAAGGTCAAG AGAGGCTGGT 1080
CCCCATGCCT TGGTTCCGAC ATCCCTGGGC ATGGGGGTGT CCTGGGGGAG ACGTGTGTCT 1140
GCCCAGGTTC CACGGGCACC TCTTGCTGTG ACTGAATCAG GGTGTGAGGC CCCAGATCTC 1200
AGGCTGTGCC TTGGGGAGGC CTGGGGCCCA GCTGTGAGTG GTTTCACAGT CCACTGAGGG 1260
AGGCTGAGGG TTTTGGGAGC CACAAATAAC CAACCTTCCC CTTCCCTCCC 1310
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