Tag | Content |
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EnhancerAtlas ID | HS048-00022 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:1172450-1174130 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxa2 | MA0047.2 | chr1:1172971-1172983 | CCAGAGTAAACA | - | 6.11 | PLAG1 | MA0163.1 | chr1:1173433-1173447 | GGGGCCCAAGGGGT | + | 6.47 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41703 | chr1:1170354-1174245 | LNCaP |
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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 |
GH01I001235 | chr1 | 1170967 | 1178914 |
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Enhancer Sequence | TGCCCTCCGC ACCCTCCCTG CTAGATGCTG GTGCCGCTAG CCCTGCCCTG ATGGCCACAC 60 TGCACCACGC TGGCCAGGTC AGAACCACCC GAGGAGAAGA ACCAAGATCT GGCCCCACCC 120 TGTCCTCCTC GGAAGGTCTC TCTGGGGCCC ACCCCCTCCT CCCTCCCCAA GGATCTGAGC 180 CTCCCTCACC GAGGTTCCCA GTGGAGGTAG ACAGTGGATG AGTGATCCCA GGAGAGCTGG 240 CTGCAGCCAA GGGGCTGAAG GGAGGTGGAG GCGGGAGGGG CAGGAAGGAG GATCTGGAAG 300 GCCCCAGGCG CTCCCCACCC ATCCAGCCTC GGCCTCTGTC CTGGTCGCGT TGCCCAGCGA 360 GGCCTCTCCT TGGGCTGGGG CTCGGGTACT CTGCCCTGGT CGGGGCCACA GATGCCGCAA 420 AGTCCCCTCA ACTCAGCTAG CCAGGGTGCA AGACCGCGCC CACAGCTGAG AAGCCAGGGG 480 TTACGAGTGT GGCCCTGCCA GGACCTCCTC AGCTGCATCC TCCAGAGTAA ACACAGGTGG 540 CCGCAGATCT TCCAGGGCCG GCCGGGCAGG CAGGACAGGA GCCCAGGAGG GCCGCAGTCC 600 AGCTCCCCTC CCCGCTGACC CAGGGCCGGA CCCAGCCCGG TGACTGGAGC AGAAGGAAAC 660 CCAAGCCCCA GGCCCTCCCT CCGGTGGCAT CCGAAGGTCT CAGCGGCCCC AGCCTCCCCC 720 AGGGGCCCCG CACCCGCCAC CGCCCACCTC AGACCGGAGA GAGAGTGAGG GATGGGCAGA 780 GCCAGGCCCA AGTCCCCGCC GGGGCGACGG TCACGGTGCC TCACCCTCAA CCGCCTCACC 840 CAGACCTTCC GACCCAGGAA CAGCTGAACT CAGCCTAAAA AGCACCCGTC CCGAGGGCCT 900 GAGTCCGGCC GTGGTGCCTC CTGCTGCAGA GATGTGTTTT GCACACTCCT GTGTGGCAGG 960 GAGAGGCCCG GGCGTGCGGG CTGGGGGCCC AAGGGGTCTG GAGACGCTTC CCTGCGGAGA 1020 CGGGGTTTGC CCAGCCCCCA CCTGTCACGC TTCTCGTCAC CCCCAAGTGA GGGCCGTGGG 1080 CGCGGGCGGG GTGGGCAGGA GGCCCTGCTG GGCTGGGTCA CACGCATGAC ACCTGGCTGT 1140 CGCAACACAG ATATCATCAC GCCCGGGCAC CCGTGAGTCA CTGGCCCAGA GCAGGGGCTG 1200 CCCCCAGCCT CCCAAACAAA GACCCTTTGT CCCCAGGCCT CTGGTGCCAG GCCCACCTGT 1260 ACAGCAGTCA GATGCGCAGG CGGACAGACA CGCCGGTGGC TCGGCAGGCA CAGGCAGGGC 1320 CAGGGCGTGT TCCCGCAACC AGACACGCTG CCATTCCTGG GTCAGGGTCA GGCTGAGGGA 1380 GACCCCTGGG GGACAGGCCC TGAGGTCACC ATAGCTCAGA GTGACCTGAA CTGGGAGTCC 1440 AAGCACAGAC TGGCCAAGCC CAGCCCGTGA GCGACGGCCC CAGGACGCGG CGCCGAGCTC 1500 TGCCCCCAGC TCCAGCTCCC AGCGGCGTCG GAGCACAGCA GATCCCAGGG CAGCGCTCTG 1560 CAGGCAGGAA AGAGCTTCCC CTTGGGACAG CGCGCTGAGC AGCCCCCAGC TGAGGGTGGG 1620 AGCCCCGTCC CTGGACCCCT TCACGCAGTT CAGGGAGCCC CACATGCCGA AGCAGCCGTC 1680
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