Tag | Content |
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EnhancerAtlas ID | HS098-10499 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:68933710-68934540 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr11:68934161-68934172 | GATGAGTCACT | - | 6.02 | JUND | MA0491.1 | chr11:68934161-68934172 | GATGAGTCACT | - | 6.32 | MEF2A | MA0052.3 | chr11:68934175-68934187 | TCTAAAAATAAA | + | 6.07 | MEF2C | MA0497.1 | chr11:68934173-68934188 | GTTCTAAAAATAAAA | + | 6.47 | Myod1 | MA0499.1 | chr11:68934071-68934084 | AGGGGCAGCTGCA | - | 6.22 | NFKB1 | MA0105.4 | chr11:68934239-68934252 | AGGGGGATCCCCA | + | 6 | ZEB1 | MA0103.3 | chr11:68934299-68934310 | CGCACCTGCCC | + | 6.02 |
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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 |
GH11I069166 | chr11 | 68933484 | 68934765 |
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Enhancer Sequence | GGGAAAGGGG TGGCTCTTCT GGGTCCCCAG ACTGCTCCCA GCTTTTCCTC TGTGGAGGCA 60 GGTATGTGAG AAAGGATGCA GCCAGGCAGG TGCAACACAC CTGGGCAGCC CGTGGCTGTG 120 GCCATGGCCA TGGCCGGTCT GCATGTGGAG GAAAAGATGG TGAGGTGAGA CCCTGAGAAA 180 CAACTCTCTG ATCTCATCCA CCTCTCCCCT CCTAGGCGGG ACGAGATGGA TGCACCCTCT 240 GCCGCAGCCA CCTCTTCTGC AGGTGCCCGG CTTCTCCAGA CTTGCTATTT TGGAGGGGCA 300 GGTCAGTGGG AACGACCGAC TGCCTTGCAT CTCAGCCACT CATGGGCCTC AGAGTGTGGG 360 CAGGGGCAGC TGCAGCCCTC TCGAGCCTCT CACTCCCTGC TTGGCCTCTG TAAGCCTGTC 420 CGGGAGCAGC TCACAGAGCC CCTGTGGTGG AGATGAGTCA CTTGTTCTAA AAATAAAAGA 480 AGTGAAGTCA TGAAATAGTG TATTTCCTTT TTAAGCCCGA TGTGCCTGCA GGGGGATCCC 540 CAGCAGTGTG CTGGCGGCAG GGACCCTGAC AAGGTCTGGA GCCTCAGAGC GCACCTGCCC 600 CCACTTACAA GCCCCGGCCT CGGGGATTGG GTGGAGTGTC CCCTGCCTCC AACGGCTCCC 660 AGATGAGTGA GTAAAAGATG GCACGTAGAC CAGGAGCGGG GGCTGACACC TGCAATCCCA 720 GCACTTTGGG AGGCTGAGGT GGGAGGATCA CTTGAGGCCA GGAGTTTGGG GCCACCCTGG 780 GCAACATGGT GAAACCCTGT CTCTACTAAG AATACAAAAA AATTAACCAG 830
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