Tag | Content |
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EnhancerAtlas ID | HS108-07421 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:47387510-47388870 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr11:47388203-47388215 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr11:47388203-47388215 | ACTAAAAATAGA | + | 6.32 | MEF2C | MA0497.1 | chr11:47388201-47388216 | CTACTAAAAATAGAA | + | 6.57 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09161 | chr11:47385523-47388457 | CD14 | SE_11270 | chr11:47387236-47388775 | CD20 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I047363 | chr11 | 47385524 | 47388775 |
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Enhancer Sequence | GCTGGGATTA CAGGCATGAG CCACTGCACC CAGCCAACAC TGAGAGATTT TAATGAGTAC 60 TTTTATCCAC CTGACCACCA TCATTACCCA TCACCTGTCA TTCTTCATCC ACCCTACATC 120 CATCCTTCAT CCCCCCATCA TCCACCCATC TATCCTTCAT CCATCCATTC ATCATGGAAC 180 CATTATCCAT CCAACTATCA TCCAGCCAGC CAGAAATGAC CCATTCATCT TCATCTCTCA 240 TTTCCTCTCT CTAAACCAGT TCTTAATCTG GGGCCAAAGT CCTACCCACA CATCCCTAGT 300 CTTACTCACT TTTTTGGTGT CACTAACACC TGTACGTCAC CAGTATAAAA ATAAAATCAT 360 ATTCAAAACA ACCCCACAAA AAATGTCAAG CCTTAAGTGT CATTCAGCTG ACCTTATCTC 420 CTCAGAACAG AACCTCCAGC CTGAAGCCCT GGGCTCTTCC CAGGGGAGCA AAAGTGTGAT 480 CAAAACAGAG AAGAAAGATG AGGAATCAGG AAAGGAGGGG CCAAGAAAAA AACCTTCTCA 540 GAAGATCACA GACCACTAGA CTAGGGCTCC CGAAGCCCAG CCTCTCCTGA AAATTATTCA 600 GACGTAGAAA CAGGCTCAGA GGTCGAGGCA GGTGGATCAA CTGACATCAG GAGTTCAAGA 660 TCAGCCTGGC CGACATGTTG AAACCCTGTC TCTACTAAAA ATAGAAAAAA AATTAGCTGG 720 GCGTGGTGGC AGGCATCTGT AATCCCACCT ACTCAGGAGG CTGAGTCAGG AGAATTACTT 780 GAACCCAGGA GATGGAGGTT GCAGTGAGCA GAGATCGCAC CATTGCACTA CAGCCTGGAC 840 GATAAGAGTG GAACGCTGTC TCAAAAAGAA AAGAAAAGAA AAGAAAAGAA AAGAAACAGG 900 CTCAGAGAAC AGAGAACTGA AGGTTTCGGG GCACTTGTTA CTCTCTACCT TGGATTCTAA 960 TTATTAGAGT TTTAATTCTT TTCCTTGTTA CAAAGATGGA TCTTGTAGAA CCTGTGTTTT 1020 ATTCATTCCA CAGCATCTAG CAATGTGCCT GGCATATAAA AGATACTTAG TATATATTTA 1080 TTAGATGGAT AGGCCAGTGC AAGATGGAGG GCTTGGTAGG TAGAGGGAAG GATAGTTGGA 1140 AAGGTGGCTA AGTGGATGAT TAGATGGGTG TGTGAATAAA TTAATGAATG TGTAGATGGT 1200 TAGTGCTATG AAAGGATGAA GAAGTATATG GAAATTGGAT GGATAGATGG ATGGATGGAT 1260 GGATGGATAG AATTCACATT TTGGAACTCT TTTCTTCATC AATCCTATTG TAGGCCAAGC 1320 ATGGTGGCTT ATGCTTGTAA TCCCAGCACT TTGGGAGGCC 1360
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