Tag | Content |
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EnhancerAtlas ID | HS048-17037 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr17:79392290-79394600 |
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 | AACTTGATGG AGATCTGAGG CCCCCCTCTA CCACCAGTGG GCCGGGACAT GCCCCGACCC 60 AGGGCAGCTG TTCATCCCGG TGCCGCTTCA ATGCCACCTT TTGCACAGCG GAGGCCAAGA 120 GCCCTTGCCA AGGTTCAGGT CAGTAAGTGG ATAAGTCTGG TGGAGGCCTG AGCCCTGGGA 180 AGCAGCATCT TTGAGGACTT GCCCAGCTGT GTGGCTCCCA TGCCCGAGAA CAGAGTCTGC 240 CAAGGTGCGC ACACCCACAG ACGTGTGTGT GTGTACGTGT GTGTACGTGT GTGTGTACGT 300 GTGTGCGTGT GTGTGTGTAC GTGTGTGTGT GTGTGTGTGT GTAGCCACTC ATCCCAGACA 360 TGTAGCACAG TCAGACCTTG TGTGTACACC CATAGTCACG TGCATATGCC CAGAGACAGG 420 TTTGCACAGA CACACCCCGT GAGTCACACA CAGTCCCTCC CCTGCCTCTG TGCAAGTGTG 480 AGTGTGTGCA AGTGTGAGTG TGTGCAAGTG TGAGGTGCAC CCCACATCTC GAGTCTGGAC 540 CACTAGTGAT TGCAGCCAGG GTGGGGGAAG CATCACTGGG TTGTATCTGG GGGTTGAGCC 600 TGCAAACACC TGCACACCCA GCATGCACCT GCCTGTCTCC CAGCCACATC TGCACACTGG 660 GGTGGCATGT GGCTGGGCCT CTAGCCCCTG CCACAGCAGC TTCTGGTCTC CTGGTGCGGG 720 CGGAGGTCCC AGAGTGGCCT CTCACCCCAG GCAGAGCCTG GTCTCCCCAC CCCGTCCCTC 780 ATTCCTCTTT CTGGGCAGCC AAATGGTCAG ATGCTACACC CCTGCCTCCA AGCAGGCTGC 840 ACCTCCCCTC TGCATCCACG CAGGAACCTG TGCAGGGCGG CTTCCTCCCC GCGCTTTCCC 900 GGAATGAGGA ATGTGGGGCA GGGCCAGCAG GGGGGCTGCT CCTCCTTCCT GCCTCCCCTC 960 CCGTCCTGCA CAGCTCCCTT GGGAGCCTGG CTCGTGGGAA GTGTGCTTGG GACCGCCCAT 1020 CACTCCGTTC CCAGCCACTC CTGGTGTCCC CCGCCTGGGC GGGCCCTGTG GGGAGCGGGG 1080 AAGGTGTGGA GCGGAAGCCA GTGCCGAGGG AAGAGGGGAG CCTGAGTGGG TGTGGGTCGG 1140 GGGTGGGAGC TGACGCAGGC GGCGGGTGCA GCCGCCAGAC TCGGAGCCGG GGAGGCCCAT 1200 GCCAGCAGCC CGGCAGCTGG GCTTCCGGAA GCAGCGGGAG CCGGGAGCCT GGGAAGGGCC 1260 TCGCTGCTTC TCTGGAGCTG CCGCCATCTC AACGAGGCGT TTTTTTTTTT TTTTTTTTTT 1320 ACAACCCATT TCACAGTTTC CAGAAAAGGA GGATGCTGTC TCGGCGGCTC ACTTAACTCA 1380 AAACAAATGC TCGCTCTGCC GGCTCCGCGC CCGCCTCTCC CGGCTCCCGG GCCCTGCCGT 1440 CCTCTTGTTC CGTCTGCCTT CAGTCTGGTG CCACAGGGCG GAGCAGGGTC AGCCTGGCAG 1500 GAGAGTGGGG TGGGGCACAG TGGGCACCTG GCCATCCGAT TGCCCAGGCC CAGCCTCTGC 1560 TGTGTGGGTC CTCGGGACCC TGGATGGGGG CTGCTGGCAC GGCTGCTGGA CCGACCCTTA 1620 CAGAGGGAGT GGCTCTCCGG GGAGTCCTGG GCTCCAGGGC CCCAGCATGC TCTGTACCCC 1680 TCAGGCTGCC CAGCATGTGT TGCCCTTCTT AGCCATCCAT GGCAAGGAGC CTGGAAGACA 1740 GGTTGGCAGG AGGCAGGCTA GTTCCCATCG GCTGTCCTGG CCACTTAGGG CCACCTCTGC 1800 TGTAAGCCCA TGTGGCCAGC TCTCACCTAC TGTGTGCCGG CCTCCCCACA CAGCACCCCT 1860 GGGCCGGGGC CAGGCTCACT GGGCACCGAG ACTCCAGCCC AGCTGTTGTG CAGCTGTTCC 1920 CCAGTCTTCC CGCTGCTGGG CCACCCTGGG ACAGCAGGTC CAGGCACAGC CTGCCTCCTG 1980 GTCTAGTTGG CTGGACCTTG GGCTCCGGGT CAGACTGGCC TCCCAGGGAT GGGGCTGTGC 2040 CCGAGGACCT GAGCCACCTG GGGGTGGCCA CAGCCCTCCT GGTGTTGCTG TCTCCCGAAA 2100 CCATTTCCTC AGCTAGCCGG CCGCCCAAGC CAGGCCTCTA CAGCATCTTG GGCAGAGCTG 2160 AGGTGGCCCT GGAGCTGGGG CCAGAGCCCG GTCTGGATCT AGAGCTGCAA ACCCGGCCTG 2220 GGCCGGCTGG GCAGTGGGGG CAGCCAACTG GAGGCCAGTG TGCAGTCCTC GGTGGCCCCG 2280 CTGACACCGC ATCCCGCTTA CTGTCCCTTC 2310
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