| Tag | Content |
|---|
EnhancerAtlas ID | HS059-02470 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr1:114669250-114670720 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:114669439-114669457 | GGAGGGAGGGAAGACAGG | + | 6.16 |
| | | 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 |
| GH01I114126 | chr1 | 114669197 | 114670022 |
| Enhancer Sequence | GTGTTGGAGA AATCGCTTTT TGTTGATGCA TGAGCTTGTT GCCTAATGAT TTCCCATTCA 60
TCCTCTTGTA AGGGAAAGAT TAGATATTTA TTCCATCCAA AGGCACAGCA TACTAATGAG 120
GGGCACATTT GGCCGGGGGC AGGTTCGGCT TGCCCACCAG CTCTGTGCTG AAGCAGGCTG 180
CGAGCAGAGG GAGGGAGGGA AGACAGGGCT GCGGTCTGGT TGCCAGTGAG AGCCGTACCC 240
TACAGGAAGC TGGCCTGAGT GGGCAATGGG GCTGTCTGGA GGCTAGGGAA CTCATCAAGA 300
GTGAAAGTGG AACTGTCTCC ACTGTCTGGG CCTCTGGCAG CTTTGTAAGG CCATTTCTTC 360
TGAAGCAGCA GAGAAGGATC TTTTGTGAAA GGCCAAGTTT AGAAACAACT TAAATAAGAA 420
CACCCAAGGC CAGCAGAGCT GAGTAGCTCT GCTTACTGCA GGTCAGAGCC CTGTCTGGAC 480
CATTAGCTTT GTTTTCCAGC ATCACATGGG AAACCTTTAG CCCCCTGGAG CCAAGAACAG 540
CTACAGGTCC TAATTTTGGC TCAAGTGAGA GTGTGTGGAA GGGTCACCTC TGCAGCAGGA 600
ACAGTTTGTG GACTTGGAGT CCTCACCTGT GGTGGAAGGG GCCTGCTGCT GCTCAGCTGT 660
GGGAGTGTGT GACTTGACTC CTGGATTGAC CATGGAGGCC CTAGTGAAGG CTGCCCGTGG 720
GATGGAGGGT GGAACCCACA CCTCTCCTCT TTCCTTTCTG GGTTCTTGGT GGATTTTCAG 780
CAATCCTTCT CTAGAGGAGC CTTGGCCCCT TGGGCAGTCC CAGAAAAGTC AAGGTCCTGT 840
TGGCTTTAGA ACCTGGGGCT GGACACAGTG AGGCACATTC TCAGGATCTG AGCTTTGAGC 900
ATGGAGGGAC CCCTCCCTGC ACCCTCCAAC CCCCAATTTC CTCCTAGTCA CTATAGGACA 960
TGAGGTCTGA GGTTAGGGCT GCTGTTACTA TTCTGGAGCA GGAAAAGCTG CTCCTTGCTT 1020
GATGTTCCCA TCTGACCAAG AAATCCTTCC AGGGAGGCAA CCAAGCTCTT CACCTCCTCC 1080
CCTCTTTGGT GAGAGGTACA AAGGAGAGGT CCCACCCATC TCTGCATTGG CAGGAGTGGA 1140
AGGAATAAAC TGTGAGTAGG ATGCACTGGA CATTTCCAGC GATTGGCCCA AGGGAGGGGG 1200
TGCCAGAGAA TAACAAGGAT GATGAGACCA GGCCCAGGGG AGCATGGGGG CAAATGAACA 1260
TCCAGCAAAG ACAACCGGGG AGCTGCACAG CTCCCGTTGA GCAGCAAACA CACAAGGGAG 1320
CCTTGCAGCC CTACCAAGGA CCCGGTGGCT TCTGACTCAG GTGGGTGGGG GCCAGGCAGC 1380
TGGGAGGGCC ACTGCTGGGC TCACTTGGAC TGCTCAAAGA GGGCCACAGG ACTGGCCATC 1440
TTCATGCATT ATTCAGAGTG CTCCGGCTGC 1470
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