Tag | Content |
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EnhancerAtlas ID | HS165-02543 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr11:66633860-66634690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr11:66634552-66634564 | AAACAAACAAAC | - | 6.32 | MSC | MA0665.1 | chr11:66634533-66634543 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr11:66634533-66634543 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr11:66634533-66634543 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr11:66634533-66634543 | AACAGCTGTT | - | 6.02 | RREB1 | MA0073.1 | chr11:66634276-66634296 | TGTGGGTGGTTGTGAGGGGG | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 66633956 | 66634594 | chr11 | 66633975 | 66634115 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I066865 | chr11 | 66632274 | 66635318 |
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Enhancer Sequence | GGGGGAAACA TGAGGCGGGG GATAGACGAG GGGCACCGCA GCCAGTGGGG CGTCCACACA 60 CAGTGCGACT CCTGCCCATA GGCTCTGGGC CAGCCTGAAC AGCCGGTTCC TCCCAACCAG 120 TGGCTCCACC AGCCCCTGCC CTGCTCCCGC CGGGAGCCGA CTAAACTACA CAGTGCCTGG 180 CAGCTGGAGA TGGCCCGCTG AAATACCAGG ACCACCTGCT CCTGCATTCC TGACTCACGG 240 TGCCGTCCAC ACAGCCCTAA GCTGCTCCTC CCTGTACTCT GCCTCCTCCT TCCTTGAGGT 300 CTGTTTTCCC CACTCCCCTA AACTCCCCCT TGGTAAAGCC TAGATTTGAA GCCTCAGCAG 360 ATCTCTAGGT CAGAGGGCCA GGATAGCACA TTCTTGGGGC CATATGTGCT ATGCTGTGTG 420 GGTGGTTGTG AGGGGGGCAG TGTGCAAGGG AACAGGTGCT GTGAAGGCTG GGCTCCTCGA 480 AATGGTAACC ACAGCTGTGA GAGGGTTGCA CAGTGGGTGC TGGGTCAGGA CCTGTCCTTC 540 TGAGGCCTGT TTTCCTGCTG GACTTGTGCC CAAAACCCCC TAGAGATGCT TGGAGAGTGC 600 AAGCTTCCCC ACCTCTGCAG GGTTTTCCAA GCTCAGCCTT ACTGCTCCTA AGGGCAGTCA 660 CAAGTCCAAG TGGAACAGCT GTTTAAAAAA CAAAACAAAC AAACAAAAAA ACCAGGCTGG 720 GCACAGCAGG TCATGCCTGT AATCCCAGCA CTTTGGGAGG CCAAAGTGGG TGAATCCCAC 780 GAGGCCAGGA GTTCGAGACT AGCCTGGCCA ACATGGTGAA ACCCTGTCTC 830
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