Tag | Content |
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EnhancerAtlas ID | HS177-05809 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr12:112818590-112819750 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX3 | MA0684.1 | chr12:112818702-112818712 | AAACCGCAAA | + | 6.02 | ZEB1 | MA0103.3 | chr12:112819608-112819619 | CCCACCTGCCC | + | 6.14 | ZNF263 | MA0528.1 | chr12:112819553-112819574 | CGAGGAGGGAGGGAGGGAGAG | + | 6.68 |
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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 | CCAAATGTCT CGGCCAATGT GATCCGATCA CTGCCGTTTC CAGAAACACA CAGTAATGGC 60 TTTTAATTCA TTTCTATAAA TGTTCGTTGT GCGTAAAGCC AAACTGCACG CAAAACCGCA 120 AAACACAAAA GATCCCTCGC ATGCCGTTTA TAGCCAGAAG ATAGGCCATC CTCTCTGCGC 180 CCTACCCCAG AAAGCTCTCC TTACGGCAGT AAAAATTTGA TGACACCCCA TGCTACCTAC 240 ACATCAAAAT GTCATCCCAC AAAGTGGAAG GGGAGCAGTG TCAGCATCCG TTGGCCTCCA 300 TGAAACGACA CTGCCAGTAT TCCCACCTCT AGGCAAACAC GAACCCAAGT GAAGTCGATG 360 GAAAGTTCCC ACCAACCAGG CATATTTGGT TCCCTTCTGC CCCCAAGGCC AAGCAGCTCA 420 ACTGATGAGA TCTGCTGTTG CACCTGCCAC GGCTCTGAAC CCGGGATGCT TGGCGACCCC 480 CGGGGCACAC AAAAAGGCCC TGCGGCCTAA CGCGCCAGTG ACCCTTCCCC GAGAGTGCAT 540 GGAGGGCCGC TGGAGCATCC CTCTCGCTGT CCACAGCGCC CGCTTCCCTG ACAAAGGCCC 600 CGTGTCAATC CATCCGAGAC ACAACACAGA GAAGTTGCTG GATTGCCCAT CGCGGACCCG 660 CAGCTGCCAC TACCCTCTCC CGGAAAAAAA CCAAACCAAA CCAAACAAAA AAAACAGAAC 720 TAGGGAAGAA AAGGATGGGA GGGTACACAG CGTGAAAATC AAAATGTTCC CAAAGCTAAG 780 CAACCTGGGT GTGCCCTGGA AGTGGGTCCT GGGGGCCCGT GGGGGAGGGG AGGGAGGGCC 840 CGGGTGGTGG CGGTGGCTCC TCTGGGGCAT GAAGGCCGAG CCAGGCGCTA GCCTAATAAA 900 ATGCCGGGTG TCGGAACGCT CAAAAGAAAA CCACAAATGA AATCCCCTGC GGGCGCCAGG 960 CCCCGAGGAG GGAGGGAGGG AGAGCGGGGC GGGCGGTCCG CAGACCTGCG GCCGCGGCCC 1020 CACCTGCCCG CCCCGCGCCC ACACACACCT GCCCCGGCAG CCGCCGGGAG GCGAGGCCGC 1080 GGCTGAGGCG AGGAGGGGGC CCGACCCGGG GGTGCCGGGC GAGTGGGTCA GTCCGATGGC 1140 GGGGGCCGGG GGCCGCCTCG 1160
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