Tag | Content |
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EnhancerAtlas ID | HS050-32426 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr19:2653560-2654550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr19:2654044-2654055 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr19:2654147-2654158 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr19:2654045-2654055 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr19:2654148-2654158 | GGGGCGGGGC | - | 6.02 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_03374 | chr19:2654401-2654952 | Brain_Angular_Gyrus | SE_03960 | chr19:2653328-2654987 | Brain_Anterior_Caudate | SE_05100 | chr19:2652973-2655029 | Brain_Cingulate_Gyrus | SE_05956 | chr19:2653050-2655063 | Brain_Hippocampus_Middle | SE_08013 | chr19:2653344-2655232 | Brain_Inferior_Temporal_Lobe | SE_31670 | chr19:2653376-2654054 | Gastric | SE_65339 | chr19:2653110-2654684 | Pancreatic_islets |
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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: 2 | ID | Chromosome | Start | End |
GH19I002653 | chr19 | 2653799 | 2653998 | GH19I002654 | chr19 | 2654402 | 2654952 |
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Enhancer Sequence | ATGAATGTAG GGTCTCCCCC TCGGCACTGT GGGCATTGGG GCCGGATCAT TCTCTGGGGT 60 GGGGCTGTCC TGGGCACTGC GGGGAGCTGA GCAGCGTCCC TGGCCTCCAC CCACCCCATG 120 CCAGGGGCAT CCCCCATCTA GAGCTGTTCC GTTGCCTTGA ATTTCTGCCC TCTGGCCTCC 180 CCTGTCCTCA TCCTTATGGG ATCTTCAGAT GGTGCCCTTG AGGCCCAGGG CCCGTGTCCC 240 CTCCTCACTC AGCCCTCCTA TCCACAGGTG ACTCACAGTC CCCTTGGCAC CACCCAGGCG 300 CTGTCCCTGG CCTCGCCCAT GGCTAACCTT GGCAGGCATC CCCAACAGAG GCGAGGGGAC 360 AGCTCTCGCC TGCCTCGGCG AGCCCGGGTT CCAGAAGATG TGCCCAGCAC CCTGGGCCCC 420 CCACCGCCGG GTCTGGGACA CAGATGCTCT CCTCCAAACC TCCCATTCAG ACCCTCGCTG 480 TGGCGGGGGC GGGGCCGTGT CTTTTGAGAC TCTGCATATG CACGAGGGGG TGAGTTTGAG 540 TGAGGCGGTC TCCATGCAGA GGAAGGTCTT TATTTAGGAA GCCAGGTGGG GGCGGGGCCG 600 GCTGGGGAGG AGAGGCGGAG AGGAAAGACG AGCTTCTGCA GATTTCAAAC CTGTCATTTC 660 TTTTCTGACG CATACCCTCC CCTCCCGCTT CATGACAAGC TCTGTTCCCA CCTTCCCCGG 720 GTTCCCAGAG CAGCCTCCTA GACACGATCC GAAACAGCAC GGGTCCCCCT CCCAACCCCC 780 AGGCACTATG GACATTAGAG CTGGGTCACT CTCTGGGGTG GGGCCATCCT GGGCACTGCA 840 GGGAGCTGAA CAGCATCCCT GGCCTCCACC CACTCTATGC CAGGAGCACC CCCAGTCACG 900 ACAGTCACAG ATGTCCCCAG ACATTGCCTG ATGTCCCCTG GGGAACAGAA TCATCCCCAG 960 AAAGACCTCC TCAGTTAGGG GGTTCCACAG 990
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