Tag | Content |
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EnhancerAtlas ID | HS105-26041 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr14:104119150-104120550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFG | MA0659.1 | chr14:104119344-104119365 | TATCTGCTGATTCAGCTTTTC | - | 6.35 | MAFG | MA0659.1 | chr14:104119344-104119365 | TATCTGCTGATTCAGCTTTTC | + | 6.43 | MAFK | MA0496.2 | chr14:104119345-104119364 | ATCTGCTGATTCAGCTTTT | - | 6.86 | MAFK | MA0496.2 | chr14:104119345-104119364 | ATCTGCTGATTCAGCTTTT | + | 6.91 |
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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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Enhancer Sequence | CTGGCCTCTT TGTTAGTGGA GTGGAGGTGG ATTTCTGAAT AGTCTTACAG ACAACTTCCA 60 AATTTTAAAA GGAATTCAGT CTTCATATGT ATGGAAAAAG AAAATCATTT TTCCAGTGTG 120 TGATGCAGAG ACTAACGTGA CCCTATTCTC AAGCACTCAT AGCTTCACCC CAAAATCCTG 180 GAATATATAG TCTGTATCTG CTGATTCAGC TTTTCTTCCC TTCATGCAGC GTCTGTCAGT 240 CCATCCATTC ACTACATGGA CTTTCTGGGC CAGGAGCTGC CTCTAGAAGC TGTGGAGTCC 300 TACAAGATCA AGTCCCTGCC TTTTTTCTTT TTTTGGGAAT TTTTTAAAGA GACAGGGTCT 360 TGCTCCGTCA CCCAGGCTAG AGTGCAGAGG TACCATCATA GCTGACTGTC ACCTCAAATT 420 CCTGGACTCA AGCGATCCTT GTGCCTCACT GAGCCTCCTG GGTAGCAAGG AATACCTGCA 480 CATACCACCC AGCTAATTTT ACTTCATTTA TTTTTATTTA TTTATTTAGG CAGAGTCTCG 540 CTCTGTCACC CAGGCTGGAG TGCAGTAGTG AGATCTTGGC TCACTGCAAC CTCTGCCTCC 600 CGGGCTCAAG TGATTCTCGT GCCTCAGCCC CCTGAGTAGC TGGGACCACA GGCGTGTGCC 660 AGCACACTCA CCTAATTTTT GTATTTTTAG TTGAGACAGG GTTTCGCCGT GTTGGCCGGC 720 TGGTTTTGAA CTCCTGCCAT CAAGTGATCC GCCTGCCTTG GCCTCCCAAA GTGCTGGAAT 780 TATAGGAATG AGCCACCATG CCTGGCTGTC CTGCCTTTTT AAATAAGAGC TTATATTCAA 840 GGTGACATTA GACACTTAAT GAATCGTGAG ATTTTAGACA GTGGCAGTGC TGTGAAGGAA 900 ATAACTCTGA CGTGTAATCT TGCCTCCATC CCTGTCACTG TGCCGAAAAA GATCACTGCT 960 CACTATCTTT CTGTTTTTTA AACTTAACTA TGGGTTTTTA AGACTTAGAA AAAAGGAGAG 1020 AGGCTAGCAG AGGGAACCAT TGCTCAGTGA CAGCGGCTGT CAGGCACAAC AGCACAAATG 1080 ATGCTGTTTT TATATTCCCC TTTCCTCCCC CTTTTCTTTC TCACTTTGGT GTTTGAAAGC 1140 CCCTTCCAGA CATTGCATCA CATCACCCTG GGCCTGGCCC TGGTGGTGCT TCGCTGTGCC 1200 ATCCTCATCT GTGAGCCTGC CCGGTGACCG TGCTGCACCT GTCCTTGATG CCCTGTGTCT 1260 TCCAGGTCTG CTCCTCCCCT GCTGCTCTTC CTGTTCCATG TTCTTTGGCT GGTTTTTCTT 1320 TCTTCTTCCA GCTGTGTGAC TCCTTTTCAA GCCTTTGTCC AGTTAAACAT TTTACCAAGA 1380 ATGTAGTGTT CTTCCTGCAT 1400
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