Tag | Content |
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EnhancerAtlas ID | HS187-04920 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr11:111307200-111308140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR3C1 | MA0113.3 | chr11:111307896-111307913 | CAGGACACGGTGTTCCA | + | 6.05 | NR3C2 | MA0727.1 | chr11:111307896-111307913 | CAGGACACGGTGTTCCA | + | 6.03 | NR3C2 | MA0727.1 | chr11:111307896-111307913 | CAGGACACGGTGTTCCA | - | 6.06 | TFAP2C | MA0524.2 | chr11:111307669-111307681 | TGCCCTGGGGCT | - | 6.11 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_33697 | chr11:111305255-111312638 | H2171 | SE_58284 | chr11:111214563-111322309 | Ly1 | SE_58822 | chr11:111229012-111312500 | Ly3 | SE_60409 | chr11:111228279-111317704 | DHL6 | SE_60973 | chr11:111229476-111322231 | HBL1 | SE_61456 | chr11:111234062-111326162 | Toledo | SE_66961 | chr11:111305255-111312638 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 111307610 | 111307990 | chr11 | 111307551 | 111307700 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I111436 | chr11 | 111307326 | 111307925 |
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Enhancer Sequence | ATTAGCTGGG CGTGGTAGTG GGCGCCTGTA ATTCCAGCTA CTCAGGGGGC TGAGGCAGAG 60 AGAATCGCTT GAATCTGGGA GACGGAGATG GCAGTGAGCC GAGATCTCAC CATTGCACTC 120 CAGCCTGGGC AACGAGAGCA AAACTCCGTC TCAAAAAAAG AAAAAAAAAA AACAAAAGAA 180 GGGCTTTCAC CTAACAGGCC TGAGGGGTCC AGGCAGACAT GGGTGCAGAC CGTACCTGAC 240 CTTGCTGGCC CAGGGGCAGG CGGCTAGCCC AGCCCCTCCC CCGGCAGGTG CCCCTTCACC 300 TTCCCGCGCC TGCCCCTCCA GTCCACACAC CCAGGCAAGG CGCCCTCGAG CGAGCGCCGT 360 TTGTTTTGCT GAGAGTTTCC GTTGGCTCGC GTGTGGGTGT TTGTTGTATT TCTCCGGCAG 420 ATGGCAGACA GCATGCCCTC CCCACCATCA CCCCGCCCCA CCATCACCCT GCCCTGGGGC 480 TGTGTGGCAA GCAGACGCTG CAGGGCAGAA CAAAAGCCTA GCAGGTGAAC AGCCCTGTCT 540 GCGGAGACTT TTATCCAACC CAAGTCGCAG ACAATATCTT TATAAAATTC CTTTCAACTC 600 CCTCATCATC TGGAACTCTT CCTGCCTGGC TCCCAACCTG CTGCAGCCCC CAGCAGCCCC 660 CACCCTCAGA AGAACATCTG CTCCTCTGAC AGGGCACAGG ACACGGTGTT CCAAAGAGCA 720 ATTTTTTCTT TGGCTTCCAT CCACTACACC CCCTCAGAGC CCAGAGACCC CCTGCTCCCA 780 GAAGCTTCCT GCAAAACGGG AGGAGTGTAT TGATCTGTGG AATGGAGGAG ATCATTCTCC 840 TCCTCCAGTG CTCAGAACTC CTCAGCAAAA ATGACCCTCA GTTTTTACCA CCCCTGAAAA 900 ACCCCAGATG AGTCCAGGGA CTCCTGCCAG GAACTGGGTT 940
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