Tag | Content |
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EnhancerAtlas ID | HS012-14942 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr17:79392500-79394550 |
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) |
ESR2 | MA0258.2 | chr17:79394296-79394311 | GGGTCAGACTGGCCT | + | 6.24 | EWSR1-FLI1 | MA0149.1 | chr17:79393229-79393247 | TCCTCCTTCCTGCCTCCC | - | 6.08 | EWSR1-FLI1 | MA0149.1 | chr17:79393233-79393251 | CCTTCCTGCCTCCCCTCC | - | 7.49 | Myod1 | MA0499.1 | chr17:79394198-79394211 | TGCAGCTGTTCCC | + | 6.98 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_00395 | chr17:79390125-79398087 | Adipose_Nuclei | SE_01010 | chr17:79392619-79395878 | Adrenal_Gland | SE_01625 | chr17:79389351-79398706 | Aorta | SE_05872 | chr17:79388722-79398913 | Brain_Hippocampus_Middle | SE_26559 | chr17:79390386-79395974 | Esophagus | SE_28164 | chr17:79392457-79394609 | Fetal_Intestine | SE_29440 | chr17:79392485-79394550 | Fetal_Intestine_Large | SE_29667 | chr17:79391361-79395846 | Fetal_Muscle | SE_31439 | chr17:79390530-79395902 | Gastric | SE_34246 | chr17:79391602-79395908 | HCT-116 | SE_40858 | chr17:79390369-79395795 | Left_Ventricle | SE_42181 | chr17:79390117-79398205 | Lung | SE_44415 | chr17:79390147-79395782 | NHDF-Ad | SE_47177 | chr17:79391538-79395537 | Panc1 | SE_48277 | chr17:79391225-79395813 | Psoas_Muscle | SE_48718 | chr17:79390442-79395880 | Right_Atrium | SE_50245 | chr17:79389672-79395981 | Sigmoid_Colon | SE_51344 | chr17:79390313-79398121 | Skeletal_Muscle | SE_52635 | chr17:79390061-79395764 | Small_Intestine | SE_53447 | chr17:79391260-79395889 | Spleen | SE_54670 | chr17:79389831-79398114 | Stomach_Smooth_Muscle | SE_56968 | chr17:79392274-79394812 | VACO_400 | SE_65328 | chr17:79390158-79401315 | Pancreatic_islets | SE_67997 | chr17:79358663-79398404 | TC32 | SE_68398 | chr17:79359303-79407988 | TC71 |
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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 |
GH17I081416 | chr17 | 79390540 | 79398129 |
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Enhancer Sequence | GTGGCTCCCA TGCCCGAGAA CAGAGTCTGC CAAGGTGCGC ACACCCACAG ACGTGTGTGT 60 GTGTACGTGT GTGTACGTGT GTGTGTACGT GTGTGCGTGT GTGTGTGTAC GTGTGTGTGT 120 GTGTGTGTGT GTAGCCACTC ATCCCAGACA TGTAGCACAG TCAGACCTTG TGTGTACACC 180 CATAGTCACG TGCATATGCC CAGAGACAGG TTTGCACAGA CACACCCCGT GAGTCACACA 240 CAGTCCCTCC CCTGCCTCTG TGCAAGTGTG AGTGTGTGCA AGTGTGAGTG TGTGCAAGTG 300 TGAGGTGCAC CCCACATCTC GAGTCTGGAC CACTAGTGAT TGCAGCCAGG GTGGGGGAAG 360 CATCACTGGG TTGTATCTGG GGGTTGAGCC TGCAAACACC TGCACACCCA GCATGCACCT 420 GCCTGTCTCC CAGCCACATC TGCACACTGG GGTGGCATGT GGCTGGGCCT CTAGCCCCTG 480 CCACAGCAGC TTCTGGTCTC CTGGTGCGGG CGGAGGTCCC AGAGTGGCCT CTCACCCCAG 540 GCAGAGCCTG GTCTCCCCAC CCCGTCCCTC ATTCCTCTTT CTGGGCAGCC AAATGGTCAG 600 ATGCTACACC CCTGCCTCCA AGCAGGCTGC ACCTCCCCTC TGCATCCACG CAGGAACCTG 660 TGCAGGGCGG CTTCCTCCCC GCGCTTTCCC GGAATGAGGA ATGTGGGGCA GGGCCAGCAG 720 GGGGGCTGCT CCTCCTTCCT GCCTCCCCTC CCGTCCTGCA CAGCTCCCTT GGGAGCCTGG 780 CTCGTGGGAA GTGTGCTTGG GACCGCCCAT CACTCCGTTC CCAGCCACTC CTGGTGTCCC 840 CCGCCTGGGC GGGCCCTGTG GGGAGCGGGG AAGGTGTGGA GCGGAAGCCA GTGCCGAGGG 900 AAGAGGGGAG CCTGAGTGGG TGTGGGTCGG GGGTGGGAGC TGACGCAGGC GGCGGGTGCA 960 GCCGCCAGAC TCGGAGCCGG GGAGGCCCAT GCCAGCAGCC CGGCAGCTGG GCTTCCGGAA 1020 GCAGCGGGAG CCGGGAGCCT GGGAAGGGCC TCGCTGCTTC TCTGGAGCTG CCGCCATCTC 1080 AACGAGGCGT TTTTTTTTTT TTTTTTTTTT ACAACCCATT TCACAGTTTC CAGAAAAGGA 1140 GGATGCTGTC TCGGCGGCTC ACTTAACTCA AAACAAATGC TCGCTCTGCC GGCTCCGCGC 1200 CCGCCTCTCC CGGCTCCCGG GCCCTGCCGT CCTCTTGTTC CGTCTGCCTT CAGTCTGGTG 1260 CCACAGGGCG GAGCAGGGTC AGCCTGGCAG GAGAGTGGGG TGGGGCACAG TGGGCACCTG 1320 GCCATCCGAT TGCCCAGGCC CAGCCTCTGC TGTGTGGGTC CTCGGGACCC TGGATGGGGG 1380 CTGCTGGCAC GGCTGCTGGA CCGACCCTTA CAGAGGGAGT GGCTCTCCGG GGAGTCCTGG 1440 GCTCCAGGGC CCCAGCATGC TCTGTACCCC TCAGGCTGCC CAGCATGTGT TGCCCTTCTT 1500 AGCCATCCAT GGCAAGGAGC CTGGAAGACA GGTTGGCAGG AGGCAGGCTA GTTCCCATCG 1560 GCTGTCCTGG CCACTTAGGG CCACCTCTGC TGTAAGCCCA TGTGGCCAGC TCTCACCTAC 1620 TGTGTGCCGG CCTCCCCACA CAGCACCCCT GGGCCGGGGC CAGGCTCACT GGGCACCGAG 1680 ACTCCAGCCC AGCTGTTGTG CAGCTGTTCC CCAGTCTTCC CGCTGCTGGG CCACCCTGGG 1740 ACAGCAGGTC CAGGCACAGC CTGCCTCCTG GTCTAGTTGG CTGGACCTTG GGCTCCGGGT 1800 CAGACTGGCC TCCCAGGGAT GGGGCTGTGC CCGAGGACCT GAGCCACCTG GGGGTGGCCA 1860 CAGCCCTCCT GGTGTTGCTG TCTCCCGAAA CCATTTCCTC AGCTAGCCGG CCGCCCAAGC 1920 CAGGCCTCTA CAGCATCTTG GGCAGAGCTG AGGTGGCCCT GGAGCTGGGG CCAGAGCCCG 1980 GTCTGGATCT AGAGCTGCAA ACCCGGCCTG GGCCGGCTGG GCAGTGGGGG CAGCCAACTG 2040 GAGGCCAGTG 2050
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