Tag | Content |
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EnhancerAtlas ID | HS040-27835 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr5:1101940-1104870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr5:1103465-1103483 | GGAAGCAAGGAAGCCTGG | + | 6.06 | GLI2 | MA0734.2 | chr5:1102691-1102706 | CAGCGTGGGTGGTCC | - | 7.1 | RREB1 | MA0073.1 | chr5:1102988-1103008 | CCCCCACCCAACCCCACTGC | + | 7.16 | ZNF263 | MA0528.1 | chr5:1102526-1102547 | CATCCCTCCCCCTCTTCCTCC | - | 7.23 | Zfx | MA0146.2 | chr5:1104722-1104736 | CAGGCCTGGGCGGG | - | 6.74 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_23448 | chr5:1101902-1102719 | Colon_Crypt_1 | SE_23448 | chr5:1103184-1105197 | Colon_Crypt_1 | SE_23989 | chr5:1102125-1103137 | Colon_Crypt_2 | SE_23989 | chr5:1103392-1105150 | Colon_Crypt_2 | SE_24840 | chr5:1102018-1103478 | Colon_Crypt_3 | SE_24840 | chr5:1103642-1105300 | Colon_Crypt_3 | SE_28283 | chr5:1102066-1103155 | Fetal_Intestine | SE_28283 | chr5:1103691-1112207 | Fetal_Intestine | SE_29290 | chr5:1101813-1103421 | Fetal_Intestine_Large | SE_29290 | chr5:1103664-1109497 | Fetal_Intestine_Large | SE_31577 | chr5:1101801-1105240 | Gastric | SE_40750 | chr5:1098688-1112458 | Left_Ventricle | SE_41639 | chr5:1103271-1105102 | LNCaP | SE_42534 | chr5:1098973-1112501 | Lung | SE_47233 | chr5:1089215-1112103 | Panc1 | SE_47514 | chr5:1103424-1103792 | Pancreas | SE_47514 | chr5:1103979-1105101 | Pancreas | SE_48976 | chr5:1101390-1112419 | Right_Atrium | SE_49487 | chr5:1101906-1103325 | Right_Ventricle | SE_49487 | chr5:1103361-1105151 | Right_Ventricle | SE_50482 | chr5:1101838-1112417 | Sigmoid_Colon | SE_52622 | chr5:1101898-1105202 | Small_Intestine | SE_53895 | chr5:1098905-1112484 | Spleen | SE_57916 | chr5:1102152-1103075 | VACO_9m | SE_57916 | chr5:1103217-1104833 | VACO_9m | SE_61441 | chr5:1092795-1176993 | Toledo | SE_65274 | chr5:1098822-1105236 | Pancreatic_islets | SE_69167 | chr5:1097016-1105179 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 1102623 | 1102762 | chr5 | 1101948 | 1104216 |
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Enhancer Sequence | CCGCTTTGCT GAGTTTTCTC TGGCTGCAGC CGCCTGGGCA AGAGAACGTC TATCTGCTGA 60 GCATTAACAA AGGCCTGCCC CTGCTCACCG GACCTACCAA GAGCCTCCCA CCACTTCCCC 120 AGCTCCCTCC CTGCCAAGCC CCCCAGCCAC AGAGGCAACC TCCGGTCTGT TTTTCACTCT 180 AGGTTAGTTT TCCAGACACC TTATCAACAA AGTGAATGCA GACCCTGTGG TCAGTAAGCA 240 GATCCTGATG GGCTGGGCCC TTGGGGAACA GCCTCCTGGG CTTGTCCAAC CAGGCTGTGT 300 CCCCACCCCG AGAGGGAAGG AGGCGGCTGC AGGTGGAAGG GCAAAGACCA GACACACGAG 360 TGTCCCGGCC AGAGGAGGGG CAGCCCCTCC AGCCAGAGAG GCAGTGAGAG TGTGTGTGTC 420 AGATCCCTGA CCCATCCCGA TCCAGGCCTG GGAAGTGCGT TCATGGGTAG TTTCTGCAGG 480 GAGAAGCTGG CTCACCTCCC TAATCGGCCC TAATCCCCTC TGAGATCACA ATGCCTCCAT 540 CAGCCTCCCT ATCTCCAGGC ACAACCTCCT CCCTTTCTCA GTGGCTCATC CCTCCCCCTC 600 TTCCTCCCGC GTTTTGGGAT TTTACAGCCA TTCTCCGCAA AGGGCTCTAG GAACGTCCTC 660 TTAGACTCAG CCTCAGCCGG AAGCAGCTGA CAGGCAGGAG GGGCTGTGAA GCTGAAGCCA 720 GGTCCGACAG CCTCCGCCCC TTCCTGCCCT CCAGCGTGGG TGGTCCGTCC AGCTACCCAG 780 CCCTGCAGAG CAGTGGCGGG TGGCACCGGA CCTGTGCACA CAGAGAGGCG CCGGGCCTGG 840 GGCAGGGGAC AAGCAAGTCC AGGCTTCCCG GCTCCCTGCA CTCGAGGAGG TTCTCAGGCC 900 TGGCTCTGTG TGTCCCCTGG GTCCAGCAGG CCACCCTCCC CTGGAGCCAC AGGGGACTCA 960 CAGCAGAATG AGTCCCACCT GGTGACCCAG TGGCATCAGC TCACGTGGCC TCTGGGGACA 1020 GCCCGAGACT GAATGGACCC AGGAGCACCC CCCACCCAAC CCCACTGCCT GGAGGCTGAG 1080 TTCCCTGTGA AGGCGCGAGG ACCCAGGAAC ACTCCCAACC CCACTGCCTG GAGGCTGGGC 1140 TCCCTGTGAA GGTGCCGGGC ACTGAAATAA AGTGTGTTTA GGTTCCAGGA TCCGAACGCC 1200 AGCTGACGAC CCCTGGCCCT TGCCCTCCCT CTGCCCCTCA CAGTTTGTGC TGTGTGGGCC 1260 CCTAAAATCT AGAAACTGAG GCTCTCAAGG GGCACAGGAT GAGAACGGCC CAGTGTTCAG 1320 GCTGGGACAC GGGGGGCTTC AGGCAAGCTC TCAGGCTTCC AGCACAAGTT TCTGGCTAAA 1380 GCAGCGCTGC CTTCTGAGGG AAAAACAGGC CCTTCATCAC CCATTCCCGA AGTGACCTCA 1440 TCCCAACAGT CTGTGCAGAC ACCACCGCCA GTATCCTGTA AACCAGGAGA GCGCCGGGAG 1500 ATCCCAGCTC ACCGTCAGAG GCACTGGAAG CAAGGAAGCC TGGCTGGAAG GTCCTGGCAA 1560 GCTATGGCCA GACACACATG AACACACGCC ACAGAAAATA TACACTCACA TGCACAGAGA 1620 CATGCATGTG TACACATGCA CAGACAGGCA CTTCCACGTG CACACGCAAA CTTGCTCACA 1680 CGGAAGACAC TCTCCATACC CATACTCACA CGCTTCCCCC CTCATTCATA CACACAACAC 1740 TCACCTCGCA AACCTGCACA CGCACCTGTC CTCACATGTG CATACCCATA CCCGCAGTCA 1800 CATACACACA CCAACACCCG CACATACACG TGTACACACA CACATACCTG CAGCACACAC 1860 ATCTGCACAA AGTCCCAGGG GCTACAGCCC CCAGACTGCA CGACCCACGG GGCGGGGTGC 1920 CCAGGACACA GGCATGCACT GGGACTACAG CCCTTCCATC TAAAGGACAC GCCTGCTCGC 1980 GGGAAGGTGG CCTCGGGTGA ACTCACTTCC CGAACCCTCT GTCACGTGGC TGTTTGCTGG 2040 TCCTGGTCCA GCCTCCTCCC TCAGCAGCCA GAGTGACGTC TGAGCCATGG AGGGGCCGTG 2100 GGGTCCCCTA GTTCCAGAGA CTCGGGGCCC AGGCAGCCTG CAGGAGCAGA GATGAAGGAA 2160 GGCGGGAGAG GCAGGGCCCC CAGCGCACCT GCCAGGCCCT CCCAGGGCGG CTCCTGTTAC 2220 AGGCTGCCTC TGGGCTGCGG TCGGGGACCC TTGGCGGCAT GGAGGGGACC CAGGAGGGGC 2280 CTGGCCTGGC GCACTTCCCT CCTCCGATTT CCACTCCACT CAATCCCTCC CCAGTGACTG 2340 CCCAGGGCGT CTCTGAGCCT CCCTGAAAGC CCAGGCCCGA CCCGCTGGCG CCAGAGGTCT 2400 GCAGACAGAG CCAAGGAGAT GAGAGGTCAC AGCCACCGCC ACCCTCGTGA CAGGCTGGCT 2460 CCTGCCAAGG GAAACTGAGG CACAGAGCAA ATGTTCAAGG ATCACTTTAA CAACCTCCTC 2520 CCGGCTGCAC GTCTGCAAGG TGGACATCCC CTGTGCACGG GACTTAAATG GACAGGAACG 2580 CTGGGAGGGC CAGCGGGGCT ACCCCACCAT GAGGACAGCT CCAGGCCATG GCAGACACAC 2640 AAACCAGGCA TGCCAACCAA GCACACGGGC ATGCTGCGTG CGGCTATCCA TGGCCAGCCT 2700 TGGGCTCAGG TCCCAGCCCC CAAACTTCCC AGAGCCACTG TAACCACTAC AGTGGATGGC 2760 AATCTGACTC CAGGGGTCAA CACAGGCCTG GGCGGGGCCC ACTCTCATCC CGGACCCCAG 2820 GACCACTCCC CACAGAGCCG AGGCCCACCG GGGGGTGCGT GTGGGGTGCG TGTGGGGTGC 2880 TGCCCAAGAA AACCCCAGAA CGCAGGAAAC AAACCACCCC AGGTCCACAC 2930
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