Tag | Content |
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EnhancerAtlas ID | HS048-16838 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr17:74267380-74269500 |
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) |
IRF1 | MA0050.2 | chr17:74268329-74268350 | TCGTCCTTTCAGTTTTGTTTC | + | 6.05 | JUN | MA0488.1 | chr17:74268842-74268855 | ATGACATCATCAC | - | 6.87 | JUND(var.2) | MA0492.1 | chr17:74268841-74268856 | CATGACATCATCACA | - | 6.5 | PLAG1 | MA0163.1 | chr17:74268774-74268788 | GGGGCCCAGGGGTG | + | 6.27 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_10428 | chr17:74261317-74270738 | CD19_Primary | SE_11415 | chr17:74257434-74273567 | CD20 | SE_15056 | chr17:74267081-74270069 | CD4_Memory_Primary_7pool | SE_18937 | chr17:74266584-74270083 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19565 | chr17:74266473-74269954 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_21340 | chr17:74266682-74269376 | CD8_Memory_7pool | SE_23599 | chr17:74266807-74269354 | Colon_Crypt_1 | SE_24131 | chr17:74267376-74269109 | Colon_Crypt_2 | SE_24131 | chr17:74269228-74269783 | Colon_Crypt_2 | SE_24931 | chr17:74266871-74269172 | Colon_Crypt_3 | SE_24931 | chr17:74269202-74271077 | Colon_Crypt_3 | SE_27367 | chr17:74266689-74270067 | Esophagus | SE_28090 | chr17:74257585-74269455 | Fetal_Intestine | SE_29152 | chr17:74254176-74269372 | Fetal_Intestine_Large | SE_31864 | chr17:74264958-74270935 | Gastric | SE_32663 | chr17:74261503-74269696 | GM12878 | SE_43246 | chr17:74266783-74271643 | Lung | SE_47749 | chr17:74267413-74269184 | Pancreas | SE_48284 | chr17:74258480-74271528 | Psoas_Muscle | SE_50371 | chr17:74266677-74270078 | Sigmoid_Colon | SE_52552 | chr17:74254274-74270056 | Small_Intestine | SE_53757 | chr17:74260072-74269790 | Spleen | SE_55588 | chr17:74267363-74269873 | Thymus | SE_58966 | chr17:74257592-74273389 | Ly3 | SE_60322 | chr17:74239092-74270751 | Ly4 | SE_60510 | chr17:74247565-74275632 | DHL6 | SE_61026 | chr17:74257641-74276199 | HBL1 | SE_62440 | chr17:74241844-74272934 | Tonsil |
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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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Enhancer Sequence | CTGGTTTGCG GTGCTTTTAT TTCCGTTGGT GGGAAAAGCG GTCTCCTCAG AAGAGGGGTG 60 GTGGGGGTCC CTTGCCACTG GGCTGGTCTG GATGTTTTTG CTGTGGGATG GTCACACCAG 120 GGGCTCTGAC AGCAAGGTCC AGGTTGGTGT GGGGAGGAGA GAGGGGCCGG GGTCCGTCCT 180 GAGTTTCTGT GACCTTCCCT TCTTGGCCCC ATCGGTGTAG CCCCCACCCA CAGAGCCCTA 240 GTGAGAAGAG CTGGAAGCCA TTTTCATCTA CAGTGGGGAG AGCTTCCTTC TAGCTGGGGG 300 CCTCCTGATG GCCCCCCCAG GCCCTCCCAG GAAGCATCTT CCAGCTGGGC TCATCTCCGA 360 TACTCCTCTC CTCAGCTTCC CGGGGGCAGT ATGTCCCTTT GGGTCATGGC CTGTGGAGTG 420 GCCATGACCC AAAGTTCAAT TAAGGCTGGC GGGTCCCCAG AGGGGCCTGC TTCCATTCCC 480 CCTTCCCCGC AGCCCTGCAG GCGTCAGCAT GGGGCGAGGT TACCAGTTCC TGACCCAGCA 540 GCTCGTCCTC AGGTGGTCCT GCTGCTCGGG AGGTCAGCTG CGTGGGGAGC CTGTCCACCT 600 GGCTGATGGG GGTGATGGCC GCGTGGCTGG GATTCCTCCT CCAGCCCTGC CCTTCACCGC 660 CATACAGTCT GGGCAGCCCC TTCCTGTCCC GTCCTCCTGC CTCGCCCTCT GCTGGGGTCT 720 ACGGGGCCCA AGTCTTGCTG GAACACAGGC AGGACAAGGG TTCTGGAGGT TCAGGCCGGA 780 AGTGAAATAA AAGTCGAGAG GGGCCGGGCC CGGCACCCAC CGCATCCTGC CTCCGGGCCT 840 CCTCGGGCCC CTCACACGGT GGGGCAGCCC CTCCTCCAGT GGAGCGGAAC GGTGGGCCCC 900 GCTGCCCCTC CACCCCTGCG TGTGACACGG ACGTGCTTGG AAGCTGGGTT CGTCCTTTCA 960 GTTTTGTTTC CTGGTTGGAA ACCCCTGAGA CTCCTCCCCC TCCCCCCGCC CCTGCCCACC 1020 TGTGCTTTCC CAGGCTGGAA GGGGCAGCCC CTCTCAGCAC GTGGGTGGTT AGGCTGTGAC 1080 GTCCCCAGGC CTCCTGGGCC TGCACCGGGG TCCACCCAGG TGTGGGCCAT GCCCAGGTGC 1140 GGGAATGGTC GGGGGTTGCC CTGGCCGGCT TAGGGAATGT CGCTCTGGGA CCTTCTGTGG 1200 GCGTGGGGAA GGCCTGGGTG AGGAGGGCTG GGCTGCACCT CCCTGCCAAG CTGGTGAATT 1260 TGGCTTCTAG ACCCGGGAAA CTGAGCCACC TTCTGACATT TCACAGCCAG GGTGGGGCCG 1320 AGAGCAACAG GAGCCCAGCT GGAGCCTGGG AGGGGTGGCC CTGCCTCTGC CTCCTGCCCG 1380 GGGAGAAAGG GGCTGGGGCC CAGGGGTGCC CGCCCGGGGC TCCGCTGTCT GAGCAGCTCC 1440 TCTCTTCTGT CCAGCTCTGA GCATGACATC ATCACATGAA GACTCCCAGG GTCTCTGAAG 1500 AGCAGGCCAG GAGGGAGCGG CCACCCGACC CAGCCAAGCC TGCCCCGCTT TGCCCACGCG 1560 GGGGTCAGGG GCCAGAAACC TGTTTCTGGG CTGTTTCTCG CCACATTTTC CTTTCCTGTG 1620 TGATTTTGTC TCCTCACACC CCAAAGCGGG CCTCTTACTC TAGACATCCC TTTCCCATGC 1680 TGGGGAGATG GGAACTGGGG GTGGGGGGAG CCCCTTTGTC AACTCTGAGC ACTTCCTTTT 1740 CTCTGAGGAG GGAGCCTCTG AGGCAGAAAG GCTTTGGTGA CCTCAGGGCT TTATAAACCT 1800 CAGGGTGGGG GGGCCACTCT CATCTACTGG GGGACCCCTA GAATCTGGCT GGAGCCCAAG 1860 CTCAGGAGGT CAGGGGACTC CTTGGTCTCA GGAGCTTCAA GTGGGTTGCA GCAGTGATAG 1920 GGGCTCGTCT CTAGCAGTTG CTGCACTGGC CCAAGCTCAG TCTCACTTGC AGTCCTCTGT 1980 CCCCTCACCT GCCAAGACCT TTAGTGAGTC CCTTGCCTGC AGGTGTTGGG GCTAGGGCAG 2040 AGGGAAGCAA ATCACAAGCG ACAAGCGCCA GGCTCGCACC ACCTCTCCAC CCGCCGCCTG 2100 GATGTCTTTT TCTAGGAGGG 2120
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