Tag | Content |
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EnhancerAtlas ID | HS165-08639 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr2:233988840-233990310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:233989937-233989955 | GGAGAGAAGGAAGGACAG | + | 6.13 | EWSR1-FLI1 | MA0149.1 | chr2:233989933-233989951 | GGGAGGAGAGAAGGAAGG | + | 6.94 | ZNF263 | MA0528.1 | chr2:233989931-233989952 | GGGGGAGGAGAGAAGGAAGGA | + | 7.11 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09311 | chr2:233988600-233990755 | CD14 | SE_10919 | chr2:233986191-233991593 | CD20 | SE_20168 | chr2:233988759-233990188 | CD56 |
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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 |
GH02I233124 | chr2 | 233988782 | 233990284 |
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Enhancer Sequence | AGGCTTATTT CCTAAAAGAA AACCATGAGA TACCTAACCG GGCCCCTCAG TTGGCCAGGG 60 CTCTTCCTGA ATTCCAGCAG GTGGAGACTA CCAGGTCCCC CAGGCTCTCC CCGAAGAGAG 120 GAGAGATTTG TCCACAGACG CTGAGACCCT TGCCTGGCTC CTGCCTGTTC TGGGGGCTTG 180 CTGCAGGCAT CCTTTTTCTC CCTCACCTGT GGGCTGGCTT GTGGGCCACC AGGGCCCCCT 240 GCTCCCTCCC ACCCTCATGG AAACACACTT TTCATGGTTG TGCAGCTGTT CGTTTCCAAA 300 AGGACCGCAG CTCCATGGAG GCTGAAAGGG TCCCAGGCAG GCCCTGTCCC TTTTGGCCTC 360 CCTGGTCTGA GTGAGCACTG CCCTCTGGAA TCAGGAAGGT CAGGCTGTGG AAGAACTAGG 420 GCTGACCTGT CCCATTGTGA GCCCAAGGTC ACTCACCAGC ACCGCGCCCT GGCTGCACCT 480 GAACAGCTGC CCCCAGGCGC CCAGGGCCAT GCTGAGAAGC TGTTCTGCAG AAACGCCCTC 540 CACACTAAAC ACCCTCACTC CCCTCGGGCT GCCCATCCCA GCTAGTTGGG CCCCTCTGGG 600 CATGGCTGTC TGGAGGAAGA TCCCGACAAG TTTCTGTGAG GGCTGAAAAA AGAACCTCAG 660 TCTCATGACT GCTGGCTTCA CTTCCGCAAA CGAGGTCGCC CAGTTGTCGG CTCGAACCAG 720 AGCAATGCGA CATGAGGCCC GCGCAGTCCA AGAGGTCTGT TTGGGCCCAG GGCCTCTTGA 780 GGCACCGCCA GACCGTGGAG CTCGAAGCAG ACTCCTAGTT GTCTTCAGAA CCCCAGACAG 840 AGGAAGTGAA GGGCCTGTTC TCTAAAGAGG AGGTCCCCCG GGGCCCACTG TGGTTGGGCC 900 AGAGGCAGCC GCTCTGTGTG GGAAGAGGCT CAGACAGAGC TCTGGACCCT CCATTCGTGT 960 ACGTACAGAA TGAACCTTCT CCTAAAGGCG ATGGGTGGGC TCCCACCTCC CAGGCCAAGT 1020 TCAAGTCATT TGTTGAATGT CTCTGAGTGA AGGGAACCCC CTCGCTTTCT TTTATGTGTT 1080 TCTGAGAGTC TGGGGGAGGA GAGAAGGAAG GACAGAGGCT GGAGAGAGGG GACCAGGGAG 1140 AGAGGGAGAG GGGCAGTGTG GCTAGGCCTG CCTGTCTCCT TACCCCTGGT CCCCTTCCAT 1200 GGTTTTGGCC TATTCTGGGA ACTGGGCCTC TGCCTAGCCC AGGGCTCAGC CATCATGAGA 1260 CAGGTGTCTC AGCCCCTGAA AGTCTGAGAG CCAGACTCAT CCTGCTCACC TGCCTGCTGC 1320 TGTGGGCTTA GTCCATCCAA GGTCAGCAGC CCTGCAGGCC TTCCAGACCC TCCATGGAGC 1380 AAGGCCTTTT GGCCCTGGCA GGTGTTTGCT GATGGCCACA GTGGGGCAGA CACTGCACTA 1440 GCCAGGGCCC TGTGGCAGGA GGCTCTCCCT 1470
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