Tag | Content |
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EnhancerAtlas ID | HS187-01566 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:154417080-154418060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TBX20 | MA0689.1 | chr1:154417680-154417691 | AAGGTGTGAAG | + | 6.32 | TBX21 | MA0690.1 | chr1:154417680-154417690 | AAGGTGTGAA | + | 6.02 | ZNF740 | MA0753.2 | chr1:154417412-154417425 | CCGCCCCCCCCAA | + | 6.54 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_00437 | chr1:154417920-154419740 | Adipose_Nuclei | SE_09189 | chr1:154416994-154418979 | CD14 | SE_18405 | chr1:154417507-154418244 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19165 | chr1:154417350-154418048 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_26877 | chr1:154417441-154418050 | Esophagus | SE_65390 | chr1:154417214-154418384 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 154417481 | 154417982 | chr1 | 154417450 | 154417976 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I154444 | chr1 | 154417077 | 154419810 |
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Enhancer Sequence | AAAGGATGCT TGGTCAGGCG TGGTGGCTCA GGCCTATAAT CCCAGCACTT TACGAGGCTG 60 ATGGGGGAGG ATTGCCTGAG CCCAGGAGAT AGAGACCAGC CGGGCACCAT AAGGAGACCC 120 TGTCTTTACA AAAAAAAGTT AAAAAAAAAT TAGTTGGGCA TAGCAGTGCA CACCTGTAGT 180 CCTAGCTAAG TGGGAGGCTG AGGTGGAAGG ATCACCTGAG CCCAGCAGTT GGAGGCTGCA 240 ATGAGCTATG ATTGCACTAC TGCACTCCAG CCTGGGCAAC AGAGGGAGAC CCTGTCTTAA 300 CAACAAAAAG ACTCCTTAAC TGCCCCCCAC ACCCGCCCCC CCCAAATGAG GAAGGGTGAA 360 ACCTCAAAAT GAGGGGCGCT TTTGGCACCC AGACACTGTG GAGATTTGTA CACACAGCCT 420 TTTCTGTACT TGTCTCCACT AGGCTTCTCT CCACAGACCA TCCCGGGTGG CATTTGGGAC 480 CCAGCTGGAG GTGAGTCATT TCTCCTCAGG AGGCTCCTCA GTGAGGTTTA TTTATTTGTT 540 TCTACACGAA TAGAGGAGCA GTGATGAGCT GTCTGTTGGG TGGTTTAAAG GCTGCGAGGA 600 AAGGTGTGAA GTAGGGTCCC CTTGCTCAGC ACGCAGGAGC TGCCTGGCGC CACTGAGCCT 660 GTGGGTCCCA CGGTCTCTCC TCCCCTCTTC CTGTGGCTTT GTGGTTCATT ACCACTTTAA 720 CCCCAGAAAC CTGAGCCGCC AGAGGTTACT GGGCATTCTC TGGGCCACAG GCTGTGTTGG 780 GGGTCAGGAC TGAGAGTAGA AACTTTCTTC CTGAAGCATC TGTCTTGAGT ATAGTATGGG 840 GAGCCTTTAA AAAACCCTAA TGACAGCTGG GCGCGGTGGC TCACACCTGT AATCTCAGTA 900 CTTTGGGAGG CTGAGGCGGG CGGATCACCA GGTCAGGAGA TCAAGACCAT CCTGGCTAAC 960 ACGGTGAAAC CCCGTCTCTA 980
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