Tag | Content |
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EnhancerAtlas ID | HS047-19242 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:74197660-74198910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:74198282-74198300 | CTCTGCTTCCTTCCTGCC | - | 6.34 | RREB1 | MA0073.1 | chr2:74197973-74197993 | TGTGAGGGGGTGGGGTTGGG | - | 6.03 | Zfx | MA0146.2 | chr2:74198707-74198721 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_09839 | chr2:74195960-74199465 | CD14 | SE_18673 | chr2:74196877-74199162 | CD4p_CD25-_Il17-_PMAstim_Th | SE_24050 | chr2:74197915-74198407 | Colon_Crypt_2 | SE_24923 | chr2:74197864-74198328 | Colon_Crypt_3 | SE_27366 | chr2:74197681-74198516 | Esophagus | SE_32257 | chr2:74197488-74198565 | Gastric | SE_32257 | chr2:74198593-74199229 | Gastric |
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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 |
GH02I073969 | chr2 | 74196728 | 74199567 |
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Enhancer Sequence | GGTGAGGACC ATTCGGGCAG GTAGGGTGGG AAGGACGGTC CAAGCAGGGG AGCAGCATGG 60 GCAAAGGAAG GAACACACAG GATGTGATGG TGAAGGGTGG GGTGCGTCGA GGTCCTTGTG 120 GGATCAGACC TCATGCCCCT AAGCGTGATA CCACTGTGGA CCAAAATGAG TGCTGCTTCC 180 AGCTAAGGAG CTTCCTGGAT TACATGGCAT TCTAGCTGGG CATTAAGTGA AGTAGGATTT 240 TTAGAGCAAG ACTGGGTTGA GGGTGATTTG GAGTAAACAC CATAAGCAAA GGCAGGGAGC 300 TAAGAAAAGA GCCTGTGAGG GGGTGGGGTT GGGCAGGGAG ACCGCAAGGC TAGAGTAGAG 360 GGCAATAGCA GGCAAGAAAT GCTCAAATGT TTTAAATAGA GTGCTTGGCA AAGACAAGCC 420 AGGCCAGCCA AGCCTCCATT GCTCACACTG TTGTCTTATC TGTTTCTTTC AGCATTTCTA 480 CGTAGGCTGT ATCTTTGAGG CCAGAGCCCA AATGCCCGGG TCTGGAAGGA GTCTCTGAGG 540 TCCCTTGGGA GACCCAGCAA AGGGGACCGG TGTGGGACTT CTGCTCAGAA GGTGGAGGGC 600 TGGGAGAGCA GGCAGGCATT CACTCTGCTT CCTTCCTGCC TGGTGGCTGG CTGCATGCCC 660 TGAACTTGAC CTCAGATGAC CTGCGTGTTC CCTTCAGTTT CAGTGCCAGC AGCAGTGAGC 720 TTCATCTTTG GCTTTTTTTC TCCTTCAGAG CAGAGACTTT CTCTCTGCTC AAACTGGGTT 780 TTTTTTGTGG TGGTGGTGGT TGTTGTTGGC TTTTTTTTTT TTGAGATGGA GTCTCGCTTT 840 CTCACCCAGG CTGGAGTGCA GTGGTGCGAT CTCAGCTCAC TGCAATCTCC TCCTCCCAGG 900 TTCAAGTGAT TCTCCCACCT CAGCCTCCAG AGTAGCTGGG ATTACAGGCA TGCGCCACAA 960 CACCCGGCTA ATTTTGTAGT TTTAGTAGAG ACAGGGTTTC ACCACGTCGG TCAGGCTGGT 1020 CTCATACTCC TGACCTTAAG CAATCCACCC GCCTCGGCCT CCCAAAGTGC TGGGATTACA 1080 GGTGTGAGCC ACGGAGCCCG GCCTCAAACT GGTTTTTGCA GCACCAAAAA TCTCCCCAGT 1140 ACTTGGGCAG ACCTTGCCGG TGGGGTGTCT ACTGTTGTCT GCCTTTTTTC AGTTTAGAAT 1200 GATGATTTTA ATGGTGCTAG ATCATTGTAT AGGTACGTAA ATAAAGACTA 1250
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