Tag | Content |
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EnhancerAtlas ID | HS059-01480 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr1:43969670-43971080 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:43969998-43970019 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | Lhx3 | MA0135.1 | chr1:43970612-43970625 | AGCTAATTAATTT | - | 6.15 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTTGTTTTG CTTAGAACTT TTCCAATAGT TGCTGAGCAT TTAGGAAAAC CACCAGGAAC 60 AAAGCCCCTT GAGGTATTTT CGTGTCAACA CATCACAGTG TCTCAGGCTG CGTTTATGCC 120 TGTGATGTTC AGTGACTGTA CATCCACATA TAAGCCTGCG GCCCCTTCAT GATGTCTGCA 180 GTGCTGTCGT GATTGAGATC TCATCCTATA TCATGTTCCC TTTATTTCTC CTTTATGTTA 240 CTGTCGGGCC CTTATTTGGA TATTTTGACA TTTGAACATG TTGGATGTTT GAAACTATAT 300 ACATAGTAGG TAATATTATT TATGCATTTC TTTCTTTCTT TTTTTTTTTT CTTTTGAGAA 360 GGAGTCTTGC TCTGTTGCCC AGGCTAGAGT GCAGGGACGT GATCTCAGCT CACTGCAACC 420 TCCACCTCCT GGGTTCAAGC AATTCTTCTG TCTCAGCCTT CTGAGTAGCT GGTACTATAG 480 GTGCCCGCCA CCACGCCCGG CTAATTTTTG TATTTTAATA GAGATGGAGT TTCATCAAGT 540 TGGTCAGGCT GGTCTCGAAC TCCTGACCTC AAATGATCCG CCTGCCTCGG TCTCCCAAAG 600 TGCTGGGATT ACAGGCGTGA GCCACCGCGC CCGGCCTATT AATGTATTTG TTTCAAGATG 660 GTAAAGAGAA TGTTATTTGG TTGGTGCAAA ACATTTGTTA TAAATATGAA TTGGGTATGA 720 TAGACTTGAG AGCAATAAGC CTAGAAGTTA GGCAGATATC AGCAACAAGA AGGAATATTT 780 TTTGTTGTTG TTCAGAACCA TCTTACTTTT TTTTGAAACG GAGTCTTCCT CTGTCACCCA 840 GGCTGAAGTG CAGTGGTGCA ATCTCAGCTC ATTGCAACCT CTGCCTCCTG GGTTCAAGCA 900 ATTCTCCTGC CTCAGCCTCC CTAATAGCTT GCCACAATGC GAAGCTAATT AATTTTTTTT 960 TTGTATTGTA ATTTTTTTTG TATTTTTTAG TAGAGACAGG GTTTCTCCAT GTTGGCCAGG 1020 CTGGTCTCAA ACTCTTGAGT TCAAGTGATC CACCCGCCTC AGCCTAGTGC TGAGATTACA 1080 GGCATGAGCC ACCATGCCCG GCCCAGTCTT AACTTTTCTT AATAACAGAC CCATAGCAAA 1140 GACATAGGAA CTGCCTTTCA CCAGGAGTGT CAGCCTTTGA TACTGCTGGG GTGCCAAGAG 1200 CACCATGCTT CCAATTCCTC CACCTGTTAC TCTCACAAGC ATCACACCGA GACATTTCTG 1260 CTCCCCTGCC GGCCAGCCCT GGAGACGGAG AGTCCTGGCA GTGACAGACT GGCCAGGCTT 1320 GGAAAGGGCC CCTCCTCCAC TCAGCAGTGG CTTTATTGCT TGCTCAAGGC CACTGCTTTT 1380 CCCAGGATCT CCTGGAGTCC CTCCATTTTT 1410
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