Tag | Content |
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EnhancerAtlas ID | HS111-03759 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr4:2944080-2945440 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr4:2944264-2944276 | TGGCAGGGGGCG | + | 6.07 | KLF5 | MA0599.1 | chr4:2944701-2944711 | GCCCCGCCCC | + | 6.02 | Klf1 | MA0493.1 | chr4:2944615-2944626 | AGGGTGTGGCT | - | 6.02 | ZNF263 | MA0528.1 | chr4:2944474-2944495 | AGTGGAGGGGCAGGAGGGAGA | + | 6.43 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_24260 | chr4:2943353-2945707 | Colon_Crypt_2 | SE_25106 | chr4:2942265-2945823 | Colon_Crypt_3 | SE_32148 | chr4:2943177-2945807 | Gastric |
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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 |
GH04I002941 | chr4 | 2943365 | 2945320 |
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Enhancer Sequence | GAATTCCAAG TGCGACAGGA CAGAGATGGC CTGAACATTA CTGGGCTCCC AGCAGGCTCT 60 GCGGCACCGA GCCTGTGGAA GTTCACCCTC TAACAGACGC ACACCGATTT TTATGTTTCT 120 GGGTTGTGCC AGACACTGAG GGTTTCAGCG TGGGCAGGGA CACCTCAGGG GAGGGGAAAA 180 GCTTTGGCAG GGGGCGCGGT GAGAGCCAAG TGCCTGATCC TGCCTGAGAG GCCTGCTGGC 240 CACAGACTTC CTGGGGCCTA CTAGGCACAC ATGGGGCTGA TGAGGCGCTC AGGCCACATC 300 CGGGAACAGA CTGAAGTCCC TGCCCCTGTC GGGGAGACAG GCAGTGCACA GCACCCAGAG 360 GAGCAAATGG ACCAGACAGA ACACGAGAAA GGAAAGTGGA GGGGCAGGAG GGAGACAGGA 420 GAGTCAGTCG GGGGTGACGG TGGAGGGCGG GAGAGGCCTG AGGGGCAGAC GTCAGCAAAG 480 GCCTGTAGGA CGCAGGAGTC AATTCACTCG CCACGGAGAA GGGCAATCCA GGCCGAGGGT 540 GTGGCTACAC GGGGAGGGGT GGAGAGTGGG TACAGTGGGG CAGAGGTGCC GGGCCAAGCG 600 AGAGGGGAAG GCGTGGGTCA GGCCCCGCCC CACACTTCCC CAAAGCCGAG ATGCCCACCC 660 CTTCCTTGAC TCCACCTGTG CCCAGCCTGT TCCGTCACAG CCCTTCACAC GTGGGACTGC 720 AGCTATCTAC AGGTGGCTCT CCCGGAGGCA GGGAGCATGT GGGCGGCCGC GCCCCTCTGG 780 CGCCCAGCAC CGAGCCTGAC AGACAGGAGC CTTGGGAGGC AGGTGGTGGC AGAATGGGAG 840 CACTGAACCG GAAGAGTGGG CCAGACCCCT CTTGGAAGGG ACTCTGCTGG TGGTGTGAAT 900 GATGCCACAG CACCTGCTCC TCAGGTCAGT CCCCTGGACA TGCAGGCGCT TAGCACTGCA 960 CGGTGAGCTG GAAATAGAGG ACAGGGGTCT GAGCCTTGAG GTCCAACCTC TGGTCAGGCT 1020 GGGAGAGGCG TCCACAGACA TGGAAGAGCT CAGGAAGAGG CTGTGCAGCT CCTCACCCCC 1080 CAGAGGGAAG CAGCAAGTGC TGAGGAAGCA TCCAGGAGCA GGGCTGGCAT CAGGGGAAGG 1140 GGGAGGAGCA CAGGGGCTGG GGTGAGGGCC CAGGAGGGCA GCCAGTGTGC AGACTGCTCC 1200 TCATCCCAAC ACTGCTCTTG CCGCCCTCGC TCCTGAATTC AGAGCGTTAA GAGAAGCGAC 1260 ACAGCAGCGC GGCCTGTGTG AGCTGCACGA GAACTTTCAC ACTGCCTTGT CGTCACGTGA 1320 GAAAAAGTAA AAAGTTAAGA TTGATTTTAA CAATAGACCT 1360
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