Tag | Content |
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EnhancerAtlas ID | HS187-18695 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr4:89241290-89242440 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr4:89242091-89242103 | GTTTGTTTGTTT | + | 6.32 | RUNX1 | MA0002.2 | chr4:89242247-89242258 | AAACCACAGAG | - | 6.14 | SCRT2 | MA0744.1 | chr4:89241512-89241525 | GCACCTGTTGAAC | - | 6.25 |
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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 |
GH04I088318 | chr4 | 89239893 | 89242974 |
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Enhancer Sequence | AGAAAGGAAA AAAATGTTGG TAGCTCTTGC AGTGATCTAA GCAAAAATTG AGGCACTGGA 60 GAGGAGACTT ATTGAGGGGT ATGAATCAAC AGAGCTTGAT TAAGTCTAGG GGTTAAAGGA 120 GTGATTGGGT GACTGAGTGG ATAATGGTAA CAATCAAAAT AGTATCTCAA ATTCTACAAG 180 ATTCCTTTTG AGCTAGAGTT TGCTCAAAGT ACATTCAAAG CAGCACCTGT TGAACTCTGA 240 CAGCCCAGAA AAACAATAGC TAACTCACGC ATGGCTAAAT AGCTCTTAGA ATCATAGTGA 300 GTCATTGTTT TGGTTATATT AATGGATTAA TTCAGTTAAT CCTCACAAAA ACCTCATAAA 360 GTAGGCAGGA CCATATTCCA TTTTACAAAT GAGGAGATCA GTTCAGGAAA TTAGAACAGA 420 GAGGTGAACT AACTTAACCA AGGTGATATA GCCACTAAGT GTTGGAGTCT GACTTCAAAC 480 ACAGTCAGTT TTTATACTGC CTTGTTTGAA GCCTGGGGTG AAGATGGAGG TGGAGTGCTG 540 TCCTGGGAGT GGGGCTGAGG GATGCAGCAC TTTACAAGGG CAAAGTTTCC TACAAATCAC 600 CTTTAAACAT CTTTCTTCCT TCTCAAAGTT CACACTCACC CTGGCTGCCA AGTGCTCCCT 660 GCTCCTCGGG GCTATTGCTG TGCTGTTCTT GAGAGCTTCC TCCTTCCACC AGACAGTTTC 720 TGTTCCCCTT AGTTCTGAGA AATGTGGCCG TCCTGGCCTA GCACCCTCCT AGGAGAAGTG 780 AAGTCCCCTG CAGATCTTTC TGTTTGTTTG TTTTTCTGGA GCAAACAAGC CCTGCTTTCA 840 ATTCAGGGAA AGGTGGAAGG AGAACAGAGG TCTGGGAATG TGAAGAAGCT AAGACAGTGG 900 ATTTGATTGG GCACTTGTTT TGTTTGTGGT GTCTCAGGGA TATTCAACTG AAAAGAGAAA 960 CCACAGAGAT AGGAAGCCAG AAGAGGTTTG AAATTCTTTT GAAATACTTA CTAAATATTT 1020 GCTTTCAGAC ACTTTGCAGG AGTATTCAAA CAGCATCTCC CTGTATGTTG GAAAGCAGCC 1080 CGTGTACACA GCTAAATATT TTTTCTAAAT AATCTTGAAA AGGAAACTAA ACCAATCATG 1140 CATCACTGAC 1150
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