Tag | Content |
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EnhancerAtlas ID | HS050-00598 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:12004280-12005220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF13 | MA0657.1 | chr1:12004895-12004913 | AAGCCAGGCCCCTTTGTT | + | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34570 | chr1:12004366-12005693 | HCT-116 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 12004346 | 12005135 | chr1 | 12004400 | 12005200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I011943 | chr1 | 12003568 | 12005510 |
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Enhancer Sequence | CTCTGTCTCA AAAAAAAAAA ATTGTGTCTG GCACACAGAA AATGCTCGAT GAAGGTAAGC 60 CATTATTGTT GCTGTTATTG AGAAGCAGGA ACCTGAGAAA GGGGCTTTGA GCCACGCCAC 120 CCCATCCCCT TCCCCCACCC CTGCTGCTGG AGTTCAAGAG CCTGTTCCAT CAAGAATCCT 180 GAATTGCGCA TGCACGCGTA CACACACACA CACACACACA CACACACACA CTCACTCACA 240 TGCTCTCACG CTGGCTTTTT CCATCCATGA AATGTGACAC TCTTCCTGTC CCCAGCAGCC 300 CCCTGTTGCC AAGAGGGCCT CAGAGCTGGT GGCTCTGGTT CTCTTCACCT GGGGAGAGAC 360 TTCACCGTCC TGGCAGGAGC TCGGGGGAGC CCTTCCCCAA GTGTGAGCAG CATCCCTCGT 420 TTCTGGATCC CAGGTTCAGG TAGTGAGGCC TCTCCTTCCC ACACCTGCCT GGTGTATCCA 480 CCCCCTCCTC CCCCAGCACC GCAGCTAATC CCTGCCAATC CCTGCTGGGC CGCCTGGCGC 540 CAGCCCTCTG CCCTGGGGCC AGCTCCCTGC CCCGGCTACC CCTGCCCCAG CTACCCCTGC 600 CCCGCCAGCT CTGGCAAGCC AGGCCCCTTT GTTCCTACAG TCTAGGTTCC TCCTGACTTC 660 CTGAGGTGGT GGGAGGGGAG GGCCTTACCT GCCTGCTGTC AATCTGGCCA CCAGGTGAGA 720 AGTGTAAGCT GCAGACCCTC AGGGAGCTAA GACTCACCCA GGGAAACAAT GATGAGCACT 780 GCAGTGTGGG TCTTGCCTCT GTGGCTTGGA GGCCAGAGAG GGCAGGAGAA ATCCGAGAAG 840 GCTTCATAGA GGTGGAAGGG ACGTCATTGT CACTGGCCCT GGGACCTGGA GGAAGGTTAG 900 AGAAAGGAGA CACAGGCCGG GTGTGGTGGC TCACGCCTGT 940
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