| Tag | Content |
|---|
EnhancerAtlas ID | HS073-14816 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr9:136651180-136652360 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr9:136652008-136652026 | GGAAAGAAACAAGGAAAG | + | 6.24 | | TP53 | MA0106.3 | chr9:136651528-136651546 | CACATGCCTGGGCAGGTC | + | 6.03 | | TP53 | MA0106.3 | chr9:136651528-136651546 | CACATGCCTGGGCAGGTC | - | 6.28 | | ZNF263 | MA0528.1 | chr9:136652042-136652063 | GAAAGAGGGAGGGAGGAGGGA | + | 6.06 | | ZNF263 | MA0528.1 | chr9:136652046-136652067 | GAGGGAGGGAGGAGGGAGAGA | + | 6.82 |
|
| | 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 |
| GH09I133785 | chr9 | 136651101 | 136655790 |
|
Enhancer Sequence | TGCTGTACGT GCACACGTGC CTCTGTATGC ATGCATGTAT AGCTGTGTGC CCATACCCTC 60
ACGTGAGAAT ACATATGCGC TTGTGCCTTC ACCTCTGCAT GCATACTAGT GTGCTCCTGC 120
GTGCATGGGT GTGCATCTGT GCCTGCACGC GTGTCTATGC GTGTGCACCT GTGCATGAGT 180
GTGCCCAGTG CTCCTGTGAG CATGTGCACA CACACACTTG TATCTGTCCC TGCAGGTACA 240
CACATGTACT AACACGTATG ATGCACATGC ACCCATGCTG TGTGAGCTCT CCTGTGGGTG 300
CTCTCCTGTG TGTGCTCTCC TGTGGGTGCT CTCCTGTGGG TGCACACACA CATGCCTGGG 360
CAGGTCTGCA CTCCTGCCTG CGCCCATGTG CGAGGATGCT CCACCGAGTG CATATGTAGA 420
TGCATGTTAA GCGGGGGCAG GATCCCAGGA AGGATGAGCG CAGGGCCCCA CCCAGGGCCC 480
CTCCACGAGG CCTGACCACC CACTTTCACT TCCTAAATGT GATGCTAAAA AAACCTCACT 540
TCTCTGAAGT AGAACAGTAA CAACAAAAAG GCAGGGAACA GCCATGGGCC TGGGGCACCC 600
CCCGTGAAGC CATCCCCGAC TGAGCAACCC ACAACTGCCC CCTTCCCTGC CTCCCCTTCG 660
GCCACCCCAC AGGCCTCGCC ATCTCTCCGA GCTCTCGGAC AAAGGGCTTT CAAAGTGGTC 720
CAGAAAAAAG AGTTTGGCAA ATAGGAGCCT ACTGGGTTAG AAAAGATGGC GGGAAAGAGG 780
AACGAAGGGA GGGATGGAGA GGGGAAGCGT GGAGCGGGGA TGGGAGGAGG AAAGAAACAA 840
GGAAAGAGAG AGGAAAAGGG GAGAAAGAGG GAGGGAGGAG GGAGAGAACA CAGAAAAACA 900
AAAAGGATGA TGGAGAGCTG AAGAGAGACC AAGAAACCCC AGCCTCTGAC CCCGAGCTCC 960
AGGGACTGAG GATCACGGAG TTTTCCTTTC ACACTGTCTT AGCGGGCAAG CCTTTCATCA 1020
TGAATACAAA TCATTTCATC ATCGGGAAAG GGAGTGGAGG ACGAAGGACC AAGAAAACCC 1080
TGAGCCCAGC CCCTCAGGCC CCTGGGTCCC CTGGCTCCGG GCAGAAGTGC CAGCACCAGG 1140
CTGGGATGAT TGAGGCAGGT GGGAGGACCT GGGCGCTAGG 1180
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