Tag | Content |
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EnhancerAtlas ID | HS048-30052 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr5:131721200-131722710 |
Target genes | Number: 10 | Name | Ensembl ID |
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SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_18258 | chr5:131720537-131722140 | CD4p_CD25-_Il17-_PMAstim_Th | SE_25154 | chr5:131720916-131721859 | Colon_Crypt_3 | SE_25154 | chr5:131722248-131724802 | Colon_Crypt_3 | SE_26597 | chr5:131721025-131721906 | Esophagus | SE_26597 | chr5:131722022-131723211 | Esophagus | SE_54554 | chr5:131720956-131726150 | Stomach_Smooth_Muscle | SE_62219 | chr5:131721125-131837948 | 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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| Number: 1 | ID | Chromosome | Start | End |
GH05I132384 | chr5 | 131720053 | 131726700 |
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Enhancer Sequence | ACCTTGTGCC CCATGTGCCC ACTGGCAGGA TGATTTCTGT CTGGCCTTCA CTAGAGGGCA 60 GCAACAACCC ATGAATCCCT ATTTTGTCTC CCAGAGACAG GAAGCATAGA TTATAAATTA 120 TTTCAGAATG TTTTCTCCAC ACTCAAAAGA GCCAAAACAA AACAGAATCC CATGACAGCA 180 ACAGACTTGC TCTCAGCCCT GTGCTGGGTT GCCCCAAGTG TGGGGAAAAA TAGCAGTAGC 240 TGTGAGAAGA TGGGGTCCAG CATGCCCTGT AGGAAGTTCC CAAGCCTCAG GGCAGGACAG 300 TGTAGGCCCT AGTTCTGGCT GTGTGCTGCT GAAGCCTCAT GCCACAGGCA CTGGCACCAA 360 AAGCAAGAGT CCTCAGGGTA GCCACATGGA GGAAGCCAGG CTCCTTCTGC ACCACCAAGG 420 TAGAGGAGTT GAACAGGCAG AGAAGAGGCC ATTCCAGACC AAGAGGGGAA CACTGCAGAG 480 GTGCTAAGGT GGGAATCACC CCTTGCAGGT GGAGAAGGTG AGATCACCAG CCCAAGTGGA 540 GCAGAGAGCA TTTCAGGGCA TAGTGGGAGA GTAAGCCGCA CATCATGGGG CCCAGTCATG 600 ACCGAGGGTG GGGGGCGGCT ACCTGGTCCC AGCAAGGTGG AAAATAATAT CCATAGAGCA 660 CTCAAGTGCC TTGATAAACA TGCTAATTTT TTTCCTTTTT TTCTTTTCTT TTTCTTTTCT 720 TTTTTTTTCT TTTTTTTTTC TCAGACAAAG TCTCTGTTGC CCAGGCTGTA GTGCAGTGGC 780 GTGATTTCCA CTTACTGCAA CCTCCGCCTC CCCAGTTCAA GCGATTCTCA TGTCTCAGCC 840 TCCCGAGTAG CTGGGACTAC AGGTGCCTGC CACCACACTT GGCTAATTTT TTTTGTATTT 900 CTTTGGAGAG ACGGGTTTCA CTGCGTTGGC CAGGCTGGTC TGGAACTCCT AGCCTCAAAT 960 GATCCACCGG CCTTGGCCTC CTAAAGTGCT GGGATTATAG GAGTGAACCA CTGCACCTGG 1020 CCAAACATGC TATTTTAGGT AGAGTATCTG ACTAATCTGT TGGATAAATC AGGGGTAGGG 1080 TGAGGAGAGA AGAGAAGCTA AAAGGCCAGT GCAGAAGCTT CTGTTGGTGC CGGGGACAGG 1140 GAGGAGAGTG TAGCAGGGCC TGGGCTGACA TAGACATGCA CAGAAGCCAG GCTTCCGGAG 1200 CCCATCTTGC ACCCATCTCC TCAGCCCAGC AGATGGCAAC ACTGCTCTTC AGAAATGGAG 1260 GTGGCCAGCC AGCATGGGGA TGCCGTCAGG GGGTGCAGGG CTCTCCCATT TTTGTGCGGT 1320 GTGGGGTACA CATAAGCTCA TCCACCCCAG GTTATTGCTG CGTGTGGATC AGCTCTTTGC 1380 TTCTGGCTTG TGATCACCAA ACATTCCACA AGCTCTGGTT CTGCAACCTT ATTCCCACCT 1440 ATGGCTGTGC TCTACCTGGT CTGTGGGTCT GCTGTTGGCA GGGAGGCCTC ACTGAGATTG 1500 GACCTTGTAC 1510
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