Tag | Content |
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EnhancerAtlas ID | HS040-01342 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:37950870-37953430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:37951953-37951973 | CCCTCCCCCACCCCCCCACA | + | 6.17 | TEAD1 | MA0090.2 | chr1:37951769-37951779 | ATGGAATGTG | - | 6.02 | ZEB1 | MA0103.3 | chr1:37951945-37951956 | CCCACCTGCCC | + | 6.14 | ZNF263 | MA0528.1 | chr1:37951491-37951512 | CTCCCCATCACCTCCTGCTCC | - | 6.3 |
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| Number of super-enhancer constituents: 37 | ID | Coordinate | Tissue/cell |
SE_00995 | chr1:37938982-37953203 | Adrenal_Gland | SE_01903 | chr1:37948265-37953245 | Aorta | SE_11493 | chr1:37938939-37953541 | CD20 | SE_17494 | chr1:37950569-37951665 | CD4p_CD25-_CD45RAp_Naive | SE_17494 | chr1:37952091-37953578 | CD4p_CD25-_CD45RAp_Naive | SE_17864 | chr1:37950020-37953616 | CD4p_CD25-_CD45ROp_Memory | SE_18659 | chr1:37951001-37951807 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19263 | chr1:37951954-37953461 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22516 | chr1:37952028-37953269 | CD8_primiary | SE_23342 | chr1:37950876-37953399 | Colon_Crypt_1 | SE_23956 | chr1:37950885-37951843 | Colon_Crypt_2 | SE_23956 | chr1:37951956-37953284 | Colon_Crypt_2 | SE_26141 | chr1:37950907-37953499 | Duodenum_Smooth_Muscle | SE_26814 | chr1:37948794-37953411 | Esophagus | SE_27863 | chr1:37952290-37953288 | Fetal_Intestine | SE_28852 | chr1:37952149-37953486 | Fetal_Intestine_Large | SE_31547 | chr1:37938860-37953351 | Gastric | SE_34808 | chr1:37949489-37953812 | HeLa | SE_36403 | chr1:37952043-37953189 | HMEC | SE_37759 | chr1:37949654-37953790 | HSMMtube | SE_41638 | chr1:37947973-37951816 | LNCaP | SE_41638 | chr1:37951911-37953293 | LNCaP | SE_42562 | chr1:37938719-37953498 | Lung | SE_45338 | chr1:37950944-37951914 | NHLF | SE_45338 | chr1:37951966-37953371 | NHLF | SE_46585 | chr1:37950638-37953471 | Osteoblasts | SE_47620 | chr1:37950334-37951789 | Pancreas | SE_48484 | chr1:37948733-37953659 | Psoas_Muscle | SE_49357 | chr1:37949273-37953284 | Right_Atrium | SE_50165 | chr1:37948804-37953471 | Sigmoid_Colon | SE_52446 | chr1:37948920-37953379 | Small_Intestine | SE_54020 | chr1:37948718-37953674 | Spleen | SE_56449 | chr1:37950785-37953592 | u87 | SE_62625 | chr1:37936685-37953308 | Tonsil | SE_64577 | chr1:37951962-37953469 | NHEK | SE_65323 | chr1:37939205-37953672 | Pancreatic_islets | SE_67957 | chr1:37950785-37953592 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 37951442 | 37951953 | chr1 | 37952009 | 37953206 |
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Enhancer Sequence | TGGGTGACAA AGTGAGACCC TGTCTCAAAA AAAAAAAAAA GGAATCCCTC CAGCATGGCA 60 GCTGAAAGGA CCACCCTACC CACCTGGTCA GCAGCAGATG CCCAGCAACC CCACCTGCCA 120 AGCCCCCGCT GTCTCTGCAC ACCACAGTGG AGCCTTGAGG CTGCCTGGAA AAAATAGGGA 180 ATGTTCTCAC CCCTCTTCCC ATCCCAGCTG CCAGCTGGCC ACAGCCTTGG GAGTTCATAC 240 TTGCTTACTT GCTTCTTGAC CAGAGCTGAA CTCTAAGCCA TTTGCTGCTT CTGCTGTGTG 300 TGGGGAGGGA TGGGCAGTGG GCAGCAGGTC CTGACTGGCT GTGCCGTGTC TGGAGGCCAA 360 GTCTGGCCCT GCTGGTTCAC TGATAAGCCC CGGCAAGGGT GGCAGAGCTC ATGTGGCAGG 420 TGCCTGAGGG GCTGGGATCT AGGGAGGACT GGTCAGTTCC ATGCCCCGCT GGCCTGAGCT 480 TGCATCCTGT GCTTTCCAGG CAGGCTTAGA TGCCCCTTCA GGCCTCTTTC TCAGTCTGCC 540 AGGCAGAGTG ACTCCGAGGC TACCAGGCCC AGTGCCCCAG CTGTGTTTCT TTCCCACGAA 600 TTGGGCTTTA ACTCCAAAGT TCTCCCCATC ACCTCCTGCT CCACTGCCCA TTCAAGCAGC 660 TTAGGTAGGT GGTATTTGCT CACAGGGCCT CAGTCTCCCC ACCTGTAAAA GGGACACAAT 720 GGTCCTTGCC TCTTTCTAGA TTTGAGAGAA TAACTCAGTT CCTGTGAAAG GAGGAGAGGG 780 AGGGGTCCTG GATTCAAGCC CCCATCACTA GCGATGCAGC CCTGGGCAAC CCACTTCCCT 840 CTCAGAGCCT CAGCTTCCTG CCTCTTCAGA GGCAGCTTCC CTCTGAGAGG GGGACAGGGA 900 TGGAATGTGA CTCCTGCATG CTGGAAAAGA TCAAATTCTG GGGAGCTGCC CCAGTTGCTC 960 TTTCCTCCTC TTGTTTTCCT GGTTCCAGGA GCCAGAAGCT GATGAGGAAA CCAGTAAGTA 1020 TGCAAATTCT GGCACTATTG GGAAATGATC CTGGGGAGCT CACAGAGGAC AGCCTCCCAC 1080 CTGCCCTCCC CCACCCCCCC ACAGGCCCCC CAACCTTGCC CTTGGGCTCT CACCAGCAGG 1140 GGCCGAACCC TGAGTTTTAT TGCGAGTTCT GTCTCGCACA CATGGGTTAA CCCCTCTTGG 1200 AGTGAAGCCA GGGTGACTAT GGCCAATCTG TCCTCAGAAA ACCTCCAGCC TCCCTAGCAG 1260 AGAGCAAACG AGCCCACAAT GGGATGAAAG ATCCCTGCTC TGGATGTCTC AGCCCAGTCC 1320 CCATCCCACT TCTCTAGAGT GGGGGAAACT CAGGAGTCCC CAAAGACCTG GGACCTAAGC 1380 TAGGAGCAGA ACTTTAGAGG TCCGGGGGAG CAGCTCTCCA ATCCCCCCAT CCCCGCCAGT 1440 GCTGCTCACA CCCCCCTCGT TGTAGTCTCC TGCAGGGGGG GACAGGTGGT GTCTGGGAAG 1500 GGGCCAGTAC TCCTCACCGC AGCTGCCACT TCCCTCATCT TCCCCCAGCA AAGCTCTCAG 1560 CCCTCCCTTC CCCATGCCTC CTGGAAAAGC CAGCATTTGT CTTCTGTACA CAGAAGGGAA 1620 AGACCCTAGC CCTGAGGGAG GTGCTGGGCA GGCCTCTACC AAGACAAGAG TGAGTGAGCA 1680 GCAGAGAAAG TGGGACTTGG GGGGCACATA TCTCTAGGAG CTGCAGGGAA GGAAGTGGTG 1740 CAATCAGCCT CAGCCCTGGG CCCAGCTGGT CCCTAGAGGA CGCTTCCCCA AAAGAAGGCA 1800 GCCCAAGGAC CCTAGCACTT TTGTCCCAGG GCTTCTCAAA CTTCTGGCTT TTTTTTTTTC 1860 TTGGACCATA GCAGAGTGGG TGGAGTAGAG GGTGGCAAGG GCCTGTTCTG GGGACCTCCC 1920 AGTTCATGGG AAGGGTGTGG GAGATTTGCC TGAAAGAGGC AGGAAGTAGG GCCCTACAAC 1980 TAAGGAAACC CAAGCCATCC CAGGCCATGG CATGTAAATC CTTCCAGCTA GTTCCTGAAG 2040 GGGAAGAGGC CCTAGGCTGT CATCCTGAGG TGTGGCCTTG TTAAGCTCCT CTCAAGGCAG 2100 CTGCTCGTGA TCTTCAACTG CTCATCCATT TAAGAGATGT CAGCAAAACG AGGTGGGAGG 2160 AAAGGATCAG GCGCCCCACC CCACACTAAG TTGGGCACAT TGCTGGGAGG TCAAGTCACT 2220 GGGAATGGTG CAAAGGCTCT AATTCTGGCT GCTCGTGGGC TGCTTGTGGG GCCGTGCCTG 2280 CCACCTGCCG GTGCTTCCTG GTACTGCTAC CCATGGAGCA GGGGCCTGCC CACCAGCTCT 2340 GGCCTGGAAA TGAAGGGCCT AGACACAAAG ATCTTCCAGC AGGATCTGAA AACAATAATT 2400 TAAGGAGAAT AACATGGGAA GTAAAGTGCT AAGCCAAAAA CAGGGAATTC TTAATGGCAT 2460 TTGCAGCTCC GCCCTGGAAA GAAACACCAG AGGTCACTGT CATGCCTTCT ACAAAGTCTA 2520 AAGCTCTAGA AACTTTCAAC TGTTCCAGGT AACAAATATC 2560
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