Tag | Content |
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EnhancerAtlas ID | HS098-59100 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:136994150-136995190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr9:136994488-136994506 | GCCAGGAAGGAAGGGAGG | + | 6.53 | EWSR1-FLI1 | MA0149.1 | chr9:136994484-136994502 | GGGAGCCAGGAAGGAAGG | + | 6.59 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I134128 | chr9 | 136993798 | 136995715 |
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Enhancer Sequence | CATGTCCTAT GGACTGCACC TCCTCTGCCC GAATTCGAGC CTGCCCACCC TTCCCATAGC 60 CCACCGTGCT GAGATCGGCC CCATGTGCCT GCCTGCCTGC CTCTAGCCGC TGGAGGCGTG 120 GTGGGGTGGC TGCTCCCTGC CTCCAAGGCT GTCCCCCAAG CTCTGTTGGC CACTGGAAGA 180 CAGCTGGGAG TAGGGCCCAG GCTGACCGCC TTGGAGAAGC CTCTTCTGCC GCATTCGTGG 240 AGATGCTCAG GCCTTAGCTG GTTTTGTGGG GAGTTAAAGA CCGCAGAGGT ATAGGGCAGG 300 GGTGGGCAGA TGGAGGGGCC GCGAGGGTCC TTGGGGGAGC CAGGAAGGAA GGGAGGTGCT 360 GGGAGCCAGA GACCAGGCCA AGGCCTCCAC CTGAGCCCGA GCCTCTCCTC TGCGTCAGCT 420 TTCCTATTTC AGGCAGCTGC TCCCCGCCTA GGGAATTCTC CGCGAGCTGT GGAAAATGCA 480 GCGGGGCGGG CCCTGCGTCT GTGGCTTTTT CCTCTCTTCC TCAGCTACCG CCCCAGGGCC 540 CGGCCTTCAG TGCCTCGGGC TGGCGAGGGC CGCCCCCCTC AAGGCTGGTA CGCGCTCGCC 600 TAATCCCACG TCACCTCTTT CCTTAGGTTA CTTATCCCCG TGGAGAGTGT GCTGCCTCTT 660 AACCAAGTCA GGGAGCGCTT CTATTTTATC CCAAAGAAAC ACTTCATCAC TGTGAAATCC 720 CAGAAACAAT GGGAACGGGC AGCGGGGCTA AAGTGCAGCT GGGGGCGCAG GAGGGAAGGA 780 ACTGGGAGCG GGTGTCGGCG TGGAGGGCGG ACCACAGAGC TGCTGTGGGG ACAGCCGCTC 840 AGGGATGATG TCCACACTTA GGGCCGGTAT GACTTCCAGG AACACGTGGC TCCTACGGAG 900 GTCTGCAGAG CAGGGGCAAG CCCCAGCCTG TATGTACTTG GCTGTGTGAC ATTGGGCAGG 960 TCACTGAGGC TCTCTGGGCC CCTCATTTTC CTCATCTACC AGAGCGTGGA GGTCTTTTAA 1020 ATCATTTTCC TCATCTGTAA 1040
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