Tag | Content |
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EnhancerAtlas ID | HS158-04090 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr1:180142690-180144010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr1:180143546-180143560 | TTTCCCCAGGGACT | + | 6.11 | EWSR1-FLI1 | MA0149.1 | chr1:180142870-180142888 | GGTATGAAGGAGGGAAGG | + | 6.47 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_31988 | chr1:180142670-180143785 | Gastric | SE_33743 | chr1:180141775-180144162 | H2171 | SE_48024 | chr1:180142922-180143747 | Pancreas |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 180142711 | 180142824 | chr1 | 180142995 | 180143648 | chr1 | 180143862 | 180143944 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I180173 | chr1 | 180142857 | 180143625 |
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Enhancer Sequence | GGAGTAAGGG CCCGGGGGAG GTCACAGGGA GCAGAAGGTT GCAGATGGGG AGAGACAGGT 60 GGCTTCTCTG CAGCCTTTGT TCCTCATGTG GGAGAGGGTA GCAGGTGGCT TCCAGATTTT 120 CTGCCTACAA ATGTCTGTAA CAAACAAGTC CTAGCTGATC ATGGTTCCTA GTGTTTAAAA 180 GGTATGAAGG AGGGAAGGGG ATGCTGGTGG TGGGTGATGA TGGTACAGTT AACATGTACC 240 AGTTCCTTGA TGTATGCACT AGGTACCATG CTAAGCACTT TAGATGTATG GTCATGGAAT 300 CCTCACAAGT CTTCAAGGTA GATGGTGTCA TCCTCATTTC AAAGATGAGA ACACAAAGGT 360 TCGGAGCAGT TGATGCGTTG CCCAAGGTCA CACAGCAAGA GCAAAGCAGA ACCAGTCCTT 420 GAACGAGGTC TGCCAGAGCC CGGGGCCTGT TCTCAGCTGC CAGCTTGGGA TAAGGCCAAA 480 CAGCTCTATC CCAAGGAGGG AGAAGGAAAC CAGTGTTTGG CTGTTGGAGG CAGAAGTCCA 540 AGGTAGTGAA AAGTGGCCCC GAGGCTAGAG TCCCACAGGA AGAAGCCTCT TCCCAGCCTG 600 CAGGCTCTCC CCTAGGCAGT TCAGTGGCCG GCTTCCAGGA CAACTCAACT GTGTTCCCTC 660 CTGAATCGGA AGAGCGCAGG CAAAAGCCTT GGCAGCTGTC TTGCCGCCTG GGCAGAAGCC 720 CAGATTGCCA GGAGTCAGGC TCTGTTCGGT CTGTCCTCTT GCCCCAAGGA GGTGACAGAC 780 TAGGCTTGGG GTGTCATGTA CATGGGAAAA GAGGACAAAG TGGTGAGTTA AATCAGCTAG 840 TCTGTAGCAA GGCATGTTTC CCCAGGGACT CAGGTCCCCG CTTCAAGAGA ACCTGTTCTG 900 GAGACCCCTT CCTTGACTGT GTCTGCTGTG CTGGGCTGGG ACTTAGTGGA CAGAGACAGC 960 AGCCTGTAAG CCCCTTTTCC CAAGTAAGGA GCAAGGGCAC ATTGACATAG AAGCAAGCTG 1020 ACATTTCCCA AGGGACGTAG GAAGTGCCTG CACTTCATGT TTTCAGATGA GTCTGCAAAG 1080 GAAAACAGCA GTGGTACTTC ATCACTCATC CATTCGATAA ATATTGGTTA GTAATTACAT 1140 GCTAGGTACT GTGCTGCATA GAAATGGCCC TCGAGGAGGA AAGTGTATGA ACTGCTGCCC 1200 ACAGGATCCA TGGATGCTTC TGAGGGGTGT GGGAGGGTAA CAGGGGAGGG AGCCAGTGTC 1260 CAGCTCCTAG AGCAACCTCC CCCCAACTCC CCCCAATTCA CCATTTTACA GATGAAGAAA 1320
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