Tag | Content |
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EnhancerAtlas ID | HS141-11300 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr2:233988980-233990450 |
Target genes | |
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 | CTGAGACCCT TGCCTGGCTC CTGCCTGTTC TGGGGGCTTG CTGCAGGCAT CCTTTTTCTC 60 CCTCACCTGT GGGCTGGCTT GTGGGCCACC AGGGCCCCCT GCTCCCTCCC ACCCTCATGG 120 AAACACACTT TTCATGGTTG TGCAGCTGTT CGTTTCCAAA AGGACCGCAG CTCCATGGAG 180 GCTGAAAGGG TCCCAGGCAG GCCCTGTCCC TTTTGGCCTC CCTGGTCTGA GTGAGCACTG 240 CCCTCTGGAA TCAGGAAGGT CAGGCTGTGG AAGAACTAGG GCTGACCTGT CCCATTGTGA 300 GCCCAAGGTC ACTCACCAGC ACCGCGCCCT GGCTGCACCT GAACAGCTGC CCCCAGGCGC 360 CCAGGGCCAT GCTGAGAAGC TGTTCTGCAG AAACGCCCTC CACACTAAAC ACCCTCACTC 420 CCCTCGGGCT GCCCATCCCA GCTAGTTGGG CCCCTCTGGG CATGGCTGTC TGGAGGAAGA 480 TCCCGACAAG TTTCTGTGAG GGCTGAAAAA AGAACCTCAG TCTCATGACT GCTGGCTTCA 540 CTTCCGCAAA CGAGGTCGCC CAGTTGTCGG CTCGAACCAG AGCAATGCGA CATGAGGCCC 600 GCGCAGTCCA AGAGGTCTGT TTGGGCCCAG GGCCTCTTGA GGCACCGCCA GACCGTGGAG 660 CTCGAAGCAG ACTCCTAGTT GTCTTCAGAA CCCCAGACAG AGGAAGTGAA GGGCCTGTTC 720 TCTAAAGAGG AGGTCCCCCG GGGCCCACTG TGGTTGGGCC AGAGGCAGCC GCTCTGTGTG 780 GGAAGAGGCT CAGACAGAGC TCTGGACCCT CCATTCGTGT ACGTACAGAA TGAACCTTCT 840 CCTAAAGGCG ATGGGTGGGC TCCCACCTCC CAGGCCAAGT TCAAGTCATT TGTTGAATGT 900 CTCTGAGTGA AGGGAACCCC CTCGCTTTCT TTTATGTGTT TCTGAGAGTC TGGGGGAGGA 960 GAGAAGGAAG GACAGAGGCT GGAGAGAGGG GACCAGGGAG AGAGGGAGAG GGGCAGTGTG 1020 GCTAGGCCTG CCTGTCTCCT TACCCCTGGT CCCCTTCCAT GGTTTTGGCC TATTCTGGGA 1080 ACTGGGCCTC TGCCTAGCCC AGGGCTCAGC CATCATGAGA CAGGTGTCTC AGCCCCTGAA 1140 AGTCTGAGAG CCAGACTCAT CCTGCTCACC TGCCTGCTGC TGTGGGCTTA GTCCATCCAA 1200 GGTCAGCAGC CCTGCAGGCC TTCCAGACCC TCCATGGAGC AAGGCCTTTT GGCCCTGGCA 1260 GGTGTTTGCT GATGGCCACA GTGGGGCAGA CACTGCACTA GCCAGGGCCC TGTGGCAGGA 1320 GGCTCTCCCT CCAGGAGGGA GTCAGCGAGG GACACGGGGA CGCAGATGGA GATCAATAAC 1380 GTGGGTGTCG TGGCCTGGAC CCCATGGGGC TGCGGTGAAG GCCGGGTTGT GCGCACAGTG 1440 TCCTCACCAA TGGCCTTCCT GCTGTTCTCT 1470
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