Tag | Content |
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EnhancerAtlas ID | HS048-02868 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr1:181011720-181013080 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr1:181011997-181012008 | AAACCACAGAA | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I181042 | chr1 | 181011724 | 181014705 |
| Enhancer Sequence | TGAGGTCGGG AGTTCAAGAC CAGCCTGGCC AACGTGGCAA AAACCCGTCT ATACTAAAAA 60 AAAATACAAA AATTAGCCAG GCGTGATGGT GGGCACCTGT AATCCCAGCT ACTTGGGAGG 120 CTGGGGCAGG GAGAATTGCC TGAAGCAGGG AGGCAGAGGC CGCAGTGAGC CGAGATCACG 180 CCACTGCACT CCAACCTGGG CGACAGAATG AGACTCTGTC TCAAAAAAGA TCCAGGTTAA 240 ATAGATTCAT ATTCATTTCA GCATATTTCA TTATTCCAAA CCACAGAAAT AAAGTGTTTC 300 ACCAACAATT TAATTCACCC AATATTTACC AAGCTACTAC CATGTGCCAA GCTCCCTGTG 360 CTAAGCTTTG CAGGAAATAC AAAGGAAAAA AGCAAAGTCC CTGTTCTTAA GTGCTTTAAG 420 ATTGAGAAGC AGGTAGAAGG TAGTAAGCAG AGGGAAACAG AAGGCAGAAT CTGGTAGCTA 480 TTGGTTTTAC GACAGAACTC ATGCTCTGAT GCAATCTCTG GCTCTTGTTT GCATAAGAAC 540 CAACACTTTT ATGAAGAGGC TCTCATGACT ACCCCAGAGG CTTCCACTGT CTTCCCTCCC 600 AACCCAAGCC CTCACCCACC ACAGGAAGGG AAGGGGGAAG TAAAAGGTCA AAGCAATACA 660 GAGGGACATT GGGACCTTAT GCTGCCCCAG CCTGTGGGAG GCCAGCCTCC ATCCTGTTCA 720 GTATTGCAGC TGACATGCAG GATAACACCT GTGAGGGAGG AGCCCATGGG GCGGGGATAC 780 CTACTCTGAA CCCTGCCAAA CTGCTACACC CCAGCTCCAG GAGCAAGGAG AAAGAAGTGC 840 TAACAATGAT TTTAATTGCT GGGCGTGGTG GCTCACATCT CTAATCCCAG CACTTTGGGA 900 GGCCAAAGTG GGAGGATCAC TTAAGGCCAG GAATTTGAGA CCAGCCTGGG CAACACAGAC 960 CCTGTCTCTA TTAAAAAGAA GTGGTGACGT GCTTATAATC CCAGCTACTC AGGAGGCTGA 1020 GGTGAGAGGA CCACTTAAGC CCAGGAATTC AAGGCTACAG TGAGCTGTGA TCATGCCGCT 1080 GCACTCCAGC TGGGCAACAG AGTAAAACCC TGTCATACAC ACACACACAT ATGCACACAC 1140 ATACATACAC TAACTAGTAC AATCAGTTGC TCTGGGAGAT ACCTCTCAGG GCCTCTTGTT 1200 TTTCCTAGTA TGCAAGGTAA GGGTACCCTG GCCTTGGGGT GGTCAGTTCT GAAAGATAAC 1260 CTGCACATTA TGAGTTATTT CATAAGCAGT TTTAGAGAAA AGAAAAATAT AAACAAACTT 1320 GTAGCACAGA AGCTAATCCA ACTATTTTGT GAGCTGATTT 1360
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