| Tag | Content |
|---|
EnhancerAtlas ID | HS051-28093 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr9:140034210-140035970 |
Target genes | | Number: 16 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr9:140034611-140034629 | CTTTCTTTCGTCCCTTCC | - | 6.03 | | Myog | MA0500.1 | chr9:140035299-140035310 | AACAGCTGCAG | + | 6.02 | | TP53 | MA0106.3 | chr9:140035155-140035173 | GACATGCCAGGGCATGTG | + | 7.32 | | TP53 | MA0106.3 | chr9:140035155-140035173 | GACATGCCAGGGCATGTG | - | 7.98 | | Tcf12 | MA0521.1 | chr9:140035299-140035310 | AACAGCTGCAG | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTCCGCCACC CACCTCCCCT CTCCTCCATC CTGCAACCCC ACACCCCCAG TTTCATTCCA 60
TCCTTTCCGT GCCCCCTTCC TCCCTGTAAG ACACCACCCC AGAGTCAGCT GGCTGCTTCC 120
GGGAGGCCTC GTCTCACTAG GAACCAAACA CCAGGGTCTG CTGGCTCCCC TATCTTGGCC 180
TGAGACCAGT CACCTGCCAC CTTGGCTGGT CCTCAGAGGG CCCCTGGGGC TCCAGGCCCT 240
GACTGGTGTG TGTAGACGTG GGGCTGGAGT GTGTCAGTGT GGGGGTGGGC ATTCCGGGTA 300
AGAGAGTAGA AGCGCCTGTC CAGCTACATG CCCGCCCTGC AGAGCTTTAA ACAGGACGGG 360
GCCTGGGGCC ATCTTTGTTT CTGCTTCCAG GTTCTCCTGC CCTTTCTTTC GTCCCTTCCC 420
CCTACCGATG GGTCCGCCTG GGAAGAGAAA TGGCTCAGGT GCCACGGCAG GACGCTTTGT 480
GGGGGTGGGA GTGGGGGTGC ACACGCGAGA GGCATCAGGG CATGGGAGCT GTCGGCAGCC 540
AGCGCTGCGG GGGAGGACGT GGCTCCTGGG ATTTTGCCTG TCGGAGCTGT CCGCCCCTGG 600
GCCGAGCGCC TGCTGAATTC CAATGAGGCT GCAAGGATCT GCAATGCAGC CCTTTATGTA 660
AGAGGCAAGA CAGACATCCA GCCTAGCACC GCTCACACGT GCCTACCTGA TGGACACACC 720
ACATCTGTGG ACACACATGC TCACACTCAC ACCAAATGTT ACATTAGCAC ACACTCATGC 780
ACCTCAGCAT CACACAATCA ATTTCATATG CTCATCTGCA CACATGCAGA TCCATTGACA 840
CCTGCTCATG TGCCACACAC GGCTTGGCAT GCATTCCCAG AGGCACGTGC AAACATGCAC 900
ATTTACACAC ATGGTTCCAG TCATTCACAC GCATGTACAC GAACAGACAT GCCAGGGCAT 960
GTGATGCACA TAACCATACC CTAGCACACG CGTGAACACC TGCATGGTCA CACACGGACC 1020
TACGGGTCTT TGCCAAGCAC CTCTGGGTGC AGGCTGGAAG CAAGAGCTGG GGGAGGGAGA 1080
ACCACTTCAA ACAGCTGCAG CTGCAGGGCC CACACCAGAG TTTTCTCAGA AATCCTCCCT 1140
CCCCACTTCA CAAGCCACCC CCGTGCCCCA GCCCAGGACA CCATGGGATG GGACTGGGGG 1200
GATGCATCTG TAGCCAGTGG CTGCAGTCAC ATATTCCATC TGGGACTGGG GAGGGACACG 1260
GAAGGTGGAC TCAGGAAATC CAGGAGGGGC CATTCCTGGG GAATTGCTTC AACTCACGCC 1320
CATGTTGCTG TCTGTCTGTG GGCATGGCCT CTGCAGCAAA GGCAATGCCT GCAGCTACCA 1380
CTCACGGAAC ACACCCCCGG CCAGGTACTG TCCTGCCACG TGGGGCCATG CAGTGCACGC 1440
CCCCATTCGC CAAAGCTCTA AGAGGCACAG GCAGACTTGG GGACAGACGC AGGTCCTTGC 1500
TGTGTGAAGG TGGTGTGGAC CACCAGCTGC CTGCCTCCCT GCCTTGGGAG GCTGGGGAGA 1560
GAGGGAGGCA TCAGCTCCAG GGGGCTGAGC CGCTGGCTTT AGATCTGCCC CATGGGGCCT 1620
TGGTCATGGG CAGGAAGGCT GGGCTGCACC CCCAATGCCT CCCTTCCCTT CCTTGAGGAT 1680
GAGGCCAGCA CTCAAAGTAA GGGCTTGGTG TTGTTCAGAC AGAGCCCGTC ACAGGCCCTG 1740
CCCCTGGAGA CACCAGCAAA 1760
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