Tag | Content |
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EnhancerAtlas ID | HS051-05591 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr12:2892720-2893640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr12:2893344-2893363 | TGCTGCCCTCTCCTGGCAA | - | 6.62 | PBX1 | MA0070.1 | chr12:2892776-2892788 | TTTGATTGATTG | - | 6.18 | Zfx | MA0146.2 | chr12:2893013-2893027 | CCGGCCTCGGCCTC | + | 6.28 |
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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 |
GH12I002784 | chr12 | 2893167 | 2893436 |
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Enhancer Sequence | GCTTCCAAGA CTCAGCTCAA GCACCTCTTC CTGCTGGCTG TGTGGGGTAT AGTTTGTTTG 60 ATTGATTGTT TTCAGACAGA GTCTAGCTCT GTCACTCAGG CTGGAGTGCA GTGGCGCGAT 120 CTCAGCTCAC TGCAACCTCT GCCTCCAGGA TTCAAGTGAT TCTCGTGCCT CAGCCTCCCG 180 AGCAGCCTGT AGGCACCAGC CACCACATCC AGCTAATCTT TGTATTTTTA GTAGCTACGG 240 GGTTTCACCA TGTTGGCCAA ACTGATCTCG AACTCCTTAC CTCAAGTGAT CCGCCGGCCT 300 CGGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACTG CGACTGGCCT CTGCTGAGTG 360 TTTTCTGATA CCCCTCCTGG GAACCCCACA CTCCCCTGAA GAGCCTTCTG CCCCAGCGCC 420 TCGCCCCGCT GGTCCTGTAT GTTTCCATGG CTGCCTCGCC CTCTTAGACC ACAGCCTCCT 480 GCAAAGTAGG GCCCCGTATC TCAGTTGGCT TTGCGCTCCC AGTGCCTGGC ACAGAGCCTG 540 GCTCCCATGA GCACTCAACG ACCCTTGAAA ATTGACCGGA ATCCCGGACA GCGCCGAGGT 600 AGCGCGGGGA ACGGGAGCGT GATCTGCTGC CCTCTCCTGG CAATGTGAAG CATTGTCCTA 660 AGCACAGACA CTTCCCTCTC CGCTGTACAA AAACAACTGC AGGATCGGGA AGCTGGAAAA 720 GGAGCTGATG GAGGATGGGG GATATGGATG CTGTCTAAGA GACAAACTGG ATTGAGGGGT 780 TGCTGAGACT CTGCCATCTC CCACACTTTT CCCACGTTCG TGGACGCAGG GGCGAGGTGA 840 GTGCTTTCAA AGGAGGATGC ATCCTCAGAG AGGCTCTCGC TCCCCCCATC AAACCCTATA 900 CTCTTGGATG AGATCTCGCT 920
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