Tag | Content |
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EnhancerAtlas ID | HS059-30641 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr22:37651930-37652760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:37651943-37651961 | GAAAGGAGGGAGGGAGGG | + | 6.17 | EWSR1-FLI1 | MA0149.1 | chr22:37651939-37651957 | GGAAGAAAGGAGGGAGGG | + | 7.01 | EWSR1-FLI1 | MA0149.1 | chr22:37651931-37651949 | GGAGGGAAGGAAGAAAGG | + | 7.88 | EWSR1-FLI1 | MA0149.1 | chr22:37651935-37651953 | GGAAGGAAGAAAGGAGGG | + | 8.03 | ZNF263 | MA0528.1 | chr22:37651932-37651953 | GAGGGAAGGAAGAAAGGAGGG | + | 6.13 | ZNF263 | MA0528.1 | chr22:37651940-37651961 | GAAGAAAGGAGGGAGGGAGGG | + | 6.24 | ZNF263 | MA0528.1 | chr22:37651944-37651965 | AAAGGAGGGAGGGAGGGAGAC | + | 6.32 | ZNF263 | MA0528.1 | chr22:37651936-37651957 | GAAGGAAGAAAGGAGGGAGGG | + | 7.17 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_58850 | chr22:37613664-37681838 | Ly3 | SE_61227 | chr22:37613918-37681610 | HBL1 |
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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 |
GH22I037253 | chr22 | 37649168 | 37651936 |
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Enhancer Sequence | GGGAGGGAAG GAAGAAAGGA GGGAGGGAGG GAGACAGAGA GAGAGAAAGA AAGAGAGAGA 60 GAGAAAGAGA GAGAGAGAGA AAGAAAGAAA ACATTGAGGG GATGCCTAGG GTGTCCCTGG 120 CTGGCACCCT GGAGTCAGAG CTGGGGAACA TTTGCGTCCA GGTCCACTCT GCCTTGGGGG 180 TCATCCTGTG TTCAGTGTCA CAAGCAAGAG AGGTGACAGG GAGGGCTGGC AGCTCTGGGC 240 AGTCCCCAGG TGCTGGAGTT GAGTCCCCAG CCTGACAGGG TTTTCCCAGA GTGGCTCTGA 300 GGTCAAATTC CGAGGAGCTG ATGGAACTCC CACTGACTGC CCCCCACCCG ATCCCCAAAC 360 CCAGCTCCCT GGGCTGACCG CCCTGGGCCA CTCTTCAGTT CCAGTCACCT CCCTACCTCT 420 AGGAGAGGAT TTTCTCTTCG AAGATCCCCC ATGAAGAATG CGGGTCCCTC TCTCCATCAG 480 GGACTTTCCT GATGAGAAAA CCAGCATTCT GCCCCCAGAG CCAGGCTCTG TGCCCCAGAC 540 ACACCCAGAT ACCAAACAGA ACCAAGCTCC CACTGCCCCA CACCTCAGGT CCCAGGAGGC 600 CCTCCCAGCG GGCCCCACAG GCCACTCTCT AACTGACGGG CTGATGAGAG CTGCCCCTCC 660 CATCCTTGAG CAGGTACACA CCCCCCACCC CTGCTTCCTA CACCTGCGCC TCAGGCCTCG 720 GTCTCAGTCC CTTCTCTGTA CACCCTCTGA GGTCGCTTCA GTCAGGCTAG TTCCCAGATC 780 TCTCTCCACT GCCTACTGGA GATGCCTCCT ACCCCCACCC AGGACACCCC 830
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